Chemical Formula | C7H6ClF |
Molar Mass | 146.57 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 177 - 178 °C |
Density | 1.23 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ether, chloroform |
Flash Point | 65 °C |
Vapor Pressure | Low at room temperature |
Odor | Pungent |
Chemical Formula | C7H6ClF |
Molar Mass | 144.573 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 170 - 172 °C |
Density | 1.196 g/cm³ (approximate) |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, ether |
Flash Point | 65 °C |
Vapor Pressure | Low vapor pressure at room temperature |
What are the main uses of Para-Fluorobenzyl chloride?
Para-Fluorobenzyl chloride, that is, p-fluorobenzyl chloride, has a wide range of main uses. In the field of organic synthesis, this is an important intermediate.
First, it can be used to prepare many fluorine-containing drugs. The introduction of fluorine atoms into organic molecules can often change the physical, chemical and biological activities of compounds. Using p-fluorobenzyl chloride as a starting material, through a series of chemical reactions, such as nucleophilic substitution, fluorobenzyl structures can be introduced into the molecular framework of drugs, which can help to develop new drugs with unique curative effects, high activity and low toxicity.
Second, it also has key uses in the creation of pesticides. By combining with the building blocks of various pesticide active ingredients, new fluorinated pesticides can be synthesized. Such pesticides may have stronger insecticidal, bactericidal, and herbicidal activities, and may have better environmental stability and selectivity due to the characteristics of fluorine atoms. They play an important role in agricultural production, ensuring crop harvests and reducing the damage of pests and diseases.
Third, in the field of materials science, it also contributes to fluorobenzyl chloride. It can participate in the synthesis of polymer materials and give special properties to materials. If it is introduced into the polymer structure, it may improve the heat resistance and chemical corrosion resistance of materials, and then be used in electronics, aerospace and other fields that require strict material properties.
Furthermore, it is indispensable in the preparation of fine chemicals. Such as the synthesis of special fragrances, dyes, etc. With the participation of p-fluorobenzyl chloride in organic reactions, fine chemicals with unique structures can be constructed to meet the needs of different industries for special functional compounds.
In summary, p-fluorobenzyl chloride plays an extremely important role in many fields such as organic synthesis, drugs, pesticides, materials and fine chemicals, and contributes greatly to the development of various industries.
What are the physical properties of Para-Fluorobenzyl chloride?
p-Fluorobenzyl chloride is an important compound in organic chemistry. It has unique physical properties and is relevant to various fields of chemical industry.
Looking at its properties, it is normally a colorless to slightly yellow liquid with a special odor. This odor is unique and may help chemists identify it in experiments. Its boiling point is about 172-174 ° C, and its boiling point is established. In separation operations such as distillation, it can be known at what temperature it can be vaporized and separated. The melting point is about -27 ° C, and it is solid at low temperatures. This characteristic needs to be taken into account during storage and transportation. < Br >
The density of p-fluorobenzyl chloride is about 1.198g/mL, which is different from that of water. This difference is significant in liquid-liquid separation experiments or industrial processes. Insoluble in water, but miscible with organic solvents such as ethanol and ether. This solubility provides various possibilities for organic synthesis. For example, in a specific reaction system, organic solvents can be used to prepare the reaction environment to promote the reaction.
Its vapor pressure and vapor density are also important properties. Vapor pressure or at a certain temperature shows a specific value, which affects its volatilization rate. In a chemical production workshop, the volatilization rate is related to the gas composition in the workshop and is related to safe production. The vapor density is greater than that of air, and the vapor may spread close to the ground after leakage, increasing the danger range. Proper ventilation and protection are required.
The above physical properties are all key factors to consider in the fields of organic synthesis, pharmaceutical research and development, and pesticide manufacturing, which affect the selection of reaction conditions, product separation and purification, etc.
What are the chemical properties of Para-Fluorobenzyl chloride?
P-fluorobenzyl chloride is also an organic compound. It has active chemical properties and is widely used in the field of organic synthesis.
P-fluorobenzyl chloride contains halogen atoms, so it has the properties of halogenated hydrocarbons. First, it can initiate nucleophilic substitution reaction. Because of the strong electronegativity of chlorine in the carbon-chlorine bond, it is easy to be attacked by nucleophilic reagents. In case of sodium alcohol, it can form ether; in case of sodium cyanide, nitrile compounds are produced. This is because the nucleophilic reagent is rich in electrons, such as oxygen, nitrogen and other atoms, and the nucleophilic attacks the carbon-chlorine bond, and the chlorine leaves with chloride ions.
Second, the reaction can be eliminated. In a strong alkali environment, p-fluorobenzyl chloride can eliminate hydrogen chloride, generate carbon-carbon double bonds, and form olefins. However, this reaction condition needs to be precisely controlled. Due to factors such as strong base strength and reaction temperature, it will affect the reaction direction, or cause nucleophilic substitution and elimination reactions to coexist.
Furthermore, due to the conjugation of the benzene ring and the fluorine atom, the benzene ring has a unique electron cloud distribution, which makes the electrophilic substitution reaction activity on the benzene ring different. Although the fluorine atom is an electron-absorbing group, it can make the electron cloud density of the benzene ring is relatively high, and the electrophilic reagents are easy to attack the ortho and para-sites, which is similar to the reaction law of conventional halogenated aromatics.
In addition, p-fluorobenzyl chloride has certain chemical stability, and may be dangerous in case of high temperature, open flame or strong oxidizing agent. When storing and using, operate according to specifications to prevent fire, explosion and other accidents. And because of its toxicity, the operation of this substance must strictly follow safety procedures to ensure personal and environmental safety.
What is the production method of Para-Fluorobenzyl chloride?
Fluorobenzyl chloride (p-fluorobenzyl chloride) is also an important intermediate in organic synthesis. There are several common methods for its preparation.
First, p-fluorotoluene is used as the starting material and is prepared by chlorination. This is the free radical substitution reaction between p-fluorotoluene and chlorine gas in the presence of light or an initiator. When the light is irradiated, the chlorine molecule absorbs light energy and cleaves into a chlorine radical. This free radical attacks the hydrogen atom at the benzyl position of p-fluorotoluene, resulting in a benzyl radical, which then interacts with the chlorine molecule to obtain p-fluorobenzyl chloride. When reacting, it is necessary to pay attention to the reaction temperature, chlorine gas entry rate and other factors. If the cover temperature is too high or the chlorine gas is introduced too fast, it is easy to cause the formation of polychlorinated by-products.
Second, use p-fluorobenzoic acid as the starting material. First reduce p-fluorobenzoic acid to p-fluorobenzyl alcohol, which can be achieved by strong reducing agents such as lithium aluminum hydride. P-fluorobenzyl alcohol reacts with chlorinated reagents, such as thionyl chloride and phosphorus trichloride, to obtain p-fluorobenzyl chloride. Taking thionyl chloride as an example, when it reacts with p-fluorobenzyl alcohol, hydrogen chloride and sulfur dioxide gas escape, and the reaction is relatively thorough, and the post-treatment is relatively simple.
Third, use p-fluorobenzaldehyde First, p-fluorobenzyl alcohol is obtained by reduction, and then chlorination is carried out, which is also the way of preparation. However, no matter what method, it is necessary to comprehensively weigh many factors such as the availability of raw materials, cost, and difficulty of reaction conditions to choose the best preparation process, so as to obtain high purity and high yield of p-fluorobenzyl chloride products.
What should be paid attention to when storing and transporting Para-Fluorobenzyl chloride?
Para - Fluorobenzyl chloride (p-fluorobenzyl chloride) is an organic compound with certain toxicity and reactivity. Special attention should be paid to the following items during storage and transportation:
First, the storage environment should be cool and dry. This substance is quite sensitive to humidity and temperature, and high temperature or humid environment can easily cause it to deteriorate or cause chemical reactions. For example, if placed in a humid place, it may hydrolyze to produce substances such as hydrogen chloride, which not only damages the quality of the product, but also may corrode the storage container. Therefore, it should be stored in a well-ventilated and cool warehouse, away from fire and heat sources.
Second, it needs to be sealed for storage. Fluorobenzyl chloride is volatile and volatile gaseous substances are harmful. Sealing can prevent volatilization from escaping. At the same time, it can avoid contact with air to prevent oxidation or other gas-phase reactions. For example, use sealed glass bottles or metal drums for storage, and ensure that the seal is tight.
Third, when storing, it should be separated from oxidants and alkalis. Because of its active chemical properties, contact with oxidants may react violently, or even cause combustion and explosion; when it encounters alkalis, it is prone to substitution or other chemical reactions. For example, it cannot be stored in the same library as oxidants such as potassium permanganate and alkalis such as sodium hydroxide.
Fourth, it is necessary to ensure that the packaging is complete and fixed during transportation. Stable packaging materials should be used to prevent the container from colliding and tipping over. For example, wooden boxes or special plastic boxes are used, and the interior is filled with buffer materials. And the transportation vehicle should be equipped with corresponding fire and leak emergency treatment equipment, just in case.
Fifth, operators need professional training and follow operating procedures. Whether it is in and out of storage during storage, or in the loading and unloading process during transportation, personnel should be familiar with the characteristics of p-fluorobenzyl chloride and operate strictly according to regulations to avoid accidents such as leakage due to improper operation.
What are the main uses of Para-Fluorobenzyl chloride?
Para - Fluorobenzyl chloride (p-fluorobenzyl chloride), this substance has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. First, it can be used to create many drugs. For example, the synthesis of certain compounds with specific physiological activities, through clever reaction steps, the structural fragments of p-fluorobenzyl chloride are connected to construct complex drug molecules, which help the research and development of medicine. Second, it also contributes to the field of materials science. It can participate in the preparation of polymer materials with special properties, and through polymerization with suitable monomers, give the material unique electrical, optical or mechanical properties. Third, it plays an important role in the synthesis of pesticides. Through rational chemical reactions, the molecular structure of pesticides is integrated to improve the control efficiency of pesticides against specific pests or diseases, and enhance their biological activity and targeting. P-fluorobenzyl chloride has critical uses in many fields such as organic synthesis, drugs, materials, and pesticides, providing important chemical raw materials and synthesis cornerstones for the development of various fields.
What are the physical properties of Para-Fluorobenzyl chloride?
Under normal circumstances, p-fluorobenzyl chloride is a colorless to pale yellow liquid, its color is clear and slightly pale, and it can be seen in the sunlight. If morning dew is attached to the tip of the grass, it is crystal clear but not dazzling.
As for its taste, it is irritating, pungent to smell, but not completely evil to smell. Its taste is so strong that it can make the nose suddenly feel uncomfortable, just like a sharp air needle that enters the nose. Although it does not cause serious harm, it can be alarming. < Br >
The boiling point of fluorobenzyl chloride is quite high, about 177-179 ° C. When placed in a specific container and heated with fire, when the temperature gradually rises, the liquid will boil, turn into curling gas, and rise in the air. At this time, the liquid can be seen rolling, if the state of a spring is surging, bubbles will rise, and the sound of bursting can be heard.
Its melting point is about -35 ° C. If it is in a low temperature environment and the temperature gradually drops to this, it will turn from liquid to solid, and the form will change from a flowing body to a solid thing, just like water turns into ice when it meets cold, and it will not stand still.
The density of this compound is about 1.194 g/mL. Compared with the same amount of water, in the container, it can be observed that it sinks underwater, because the density is higher than that of water, and it sinks naturally when it enters the water.
p-Fluorobenzyl chloride also has characteristics in solubility, slightly soluble in water, but miscible in most organic solvents, such as alcohols and ethers. If placed in alcohol, the two blend seamlessly, like water emulsion, while in water it is only slightly soluble, such as oil floating in water, with obvious stratification.
All of these are related to the physical properties of fluorobenzyl chloride. Each has its own use in the field of chemistry, and is the basis for chemical industry, scientific research and other things.
What are the chemical properties of Para-Fluorobenzyl chloride?
Fluorobenzyl chloride is also an organic compound. It is active and has a unique performance in various chemical reactions.
In terms of its chemical properties, the halogenated benzyl structure endows it with considerable reactivity. Chlorine atoms are one of the check points of its active reaction and can participate in nucleophilic substitution reactions. In this reaction, nucleophilic reagents can attack the carbon atoms attached to the chlorine atoms and replace the chlorine atoms. For example, when reacted with sodium alcohol, corresponding ethers can be formed; when reacted with sodium cyanide, nitriles can be obtained, which is an important method for growing carbon chains in organic synthesis.
Furthermore, although the fluorine atoms in the molecule are relatively stable, they also affect the properties of the molecule. Fluorine atoms are highly electronegative, which can affect the electron cloud distribution of molecules through induction effects, thereby affecting the reactivity and selectivity. For example, in some electrophilic substitution reactions, the presence of fluorine atoms can affect the localization effect of the substituents on the benzene ring, making the reaction more inclined to a specific position.
In addition, under basic conditions of para-Fluorobenzyl chloride, chlorine atoms are easily replaced by hydroxyl groups to form para-Fluorobenzyl alcohol. Under light or heating conditions, free radical reactions can occur, and chlorine atoms can be used as free radicals to initiate or participate in free radical chain reactions, which is also a way to prepare compounds with specific structures in organic synthesis. < Br >
Due to its active chemical properties, para-Fluorobenzyl chloride is widely used in the field of organic synthesis, and can be used as a key intermediate to prepare many bioactive compounds, drugs and functional materials.
What is the production method of Para-Fluorobenzyl chloride?
The method of preparing p-fluorobenzyl chloride used to follow various paths in the past. One method is to introduce chlorine atoms at the benzyl position with p-fluorotoluene as a group. This process often relies on light or an initiator to make the chlorine radical react with the benzyl hydrogen of p-fluorotoluene. The carbon-hydrogen bond of capped benzyl is affected by the electronic effect of the benzene ring, and its activity is higher than that of hydrogen elsewhere, so it is easy to be attacked by chlorine radicals. During the reaction, chlorine gas is introduced into the reaction kettle containing p-fluorotoluene. Under the light, the chlorine molecule is cracked into a chlorine radical, which then reacts with the benzyl hydrogen of p-fluorotoluene to obtain p-fluorobenzyl chloride. However, this reaction also produces by-products, such as polychlorinated compounds, so fine temperature control, chlorine control and reaction time are required to increase the yield of the main product.
Another method can be used to react with p-fluorobenzyl alcohol with chlorination reagents. Commonly used chlorination reagents, such as thionyl chloride, phosphorus trichloride, etc. Taking thionyl chloride as an example, it is mixed with p-fluorobenzyl alcohol. At a suitable temperature, the hydroxyl group is replaced by a chlorine atom to form p-fluorobenzyl chloride. This reaction mechanism is that the sulfur atom of thionyl chloride nucleophilically attacks the oxygen of the alcohol hydroxyl group to form an intermediate, and then the chloride ions leave to form halogenated hydrocarbons. The advantage of this path is that the reaction conditions are mild, there are few side reactions, and < Br >
In addition, p-fluorobenzoic acid is used as the starting material, first reduced to p-fluorobenzyl alcohol, and then chlorinated. First, p-fluorobenzoic acid is reduced to p-fluorobenzyl alcohol with suitable reducing agents, such as sodium borohydride, lithium aluminum hydride, etc., and then p-fluorobenzyl chloride is prepared according to the above chlorination method. Although this method is slightly complicated in steps, the raw materials are easy to obtain, and the reaction of each step is controllable. It is also a commonly used method in industrial production or laboratory preparation.
What are the precautions for Para-Fluorobenzyl chloride in storage and transportation?
Fluorobenzyl chloride is an organic compound. During storage and transportation, many matters should not be careless.
The first word is storage. First, it must be placed in a cool and well-ventilated place. Because of its certain volatility and chemical activity, warm or poorly ventilated places can easily cause its volatilization to intensify, or even cause chemical reactions, endangering safety. Second, keep away from fire and heat sources. This compound encounters open flames, hot topics, or the risk of combustion and explosion, so the source of heat must be far away. Third, it should be stored separately from oxidants and alkalis, and should not be mixed. Because of its active chemical properties, it can meet with oxidants or cause severe oxidation reactions; contact with alkalis may also cause unpredictable chemical reactions. Fourth, the storage place should be equipped with suitable materials to contain leaks. In case of leakage, it can be contained in time to avoid its spread and cause greater harm.
As for transportation, there are also various points. First, the transportation vehicle must be clean, dry, and free of other substances that may react with it. Second, during transportation, strict attention should be paid to protection from sun exposure, rain, and high temperature. High temperature and rain attack may affect its stability. Third, when loading and unloading, it must be handled lightly and not operated brutally. Because it is a chemical, if the packaging is damaged, it is easy to leak. Fourth, when transporting, you should follow the specified route, do not change at will, and do not stop in densely populated areas and downtown areas. This is to avoid serious harm to many people in the event of an accident. In this way, when storing and transporting para-Fluorobenzyl chloride, pay careful attention to all points to ensure safety.