Chemical Formula | C7H6ClF |
Molar Mass | 146.573 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 172 - 174 °C |
Density | 1.194 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents like ether, benzene |
Flash Point | 64 °C |
Odor | Pungent odor |
Chemical Formula | C7H6ClF |
Molar Mass | 146.573 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 174 - 176 °C |
Density | ~1.24 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ether, benzene |
Flash Point | 62 °C |
Odor | Pungent |
What are the main uses of 4-Fluorobenzyl chloride?
4-Fluorobenzyl chloride is an important raw material in organic synthesis. It is mainly used in a wide range of fields such as medicine, pesticides, and dyes.
In the field of medicine, this compound is often used as a key intermediate for the preparation of a variety of drugs. For example, in the synthesis of some antibacterial drugs, 4-fluorobenzyl chloride is involved and plays a key role in the construction of drug activity structures. Its unique chemical structure can endow drugs with specific biological activities and pharmacological properties, helping them better achieve the efficacy of treating diseases.
In the field of pesticides, 4-fluorobenzyl chloride is also indispensable. Through chemical reactions, it can be converted into various high-efficiency pesticides. Such pesticides have strong targeted and killing effects on pests, can effectively protect crops from pests and diseases, improve crop yield and quality, and make great contributions to agricultural production.
In the field of dyes, 4-fluorobenzyl chloride can be used as a raw material for synthesizing new dyes. After specific processing, dyes with bright colors and good stability can be prepared. These dyes are widely used in textile, printing and dyeing and other industries to meet people's needs for diverse colors and high quality of fabrics.
To sum up, 4-fluorobenzyl chloride occupies an important position in many chemical-related industries due to its special chemical properties, and plays an important role in promoting the development of various industries.
What are the physical properties of 4-Fluorobenzyl chloride?
4-Fluorobenzyl chloride is also an organic compound. Its physical properties are quite numerous, and I would like to describe them in detail.
Looking at its morphology, under room temperature and pressure, 4-fluorobenzyl chloride is a colorless to light yellow liquid, with a clear appearance and a special smell. Its pungent smell can make the senses aware. This is a warning sign and should be treated with caution during operation.
When the boiling point is discussed, it is about 177-179 ° C. When the temperature rises to this value, 4-fluorobenzyl chloride converts from a liquid state to a gaseous state, and the thermal motion of the molecule intensifies, breaking free from the shackles of the liquid phase. The characteristics of this boiling point are crucial in the separation and purification of chemical operations. According to its boiling point, distillation and other methods can be used to obtain pure products.
Melting point is about -33 ° C. When the temperature drops to Si, 4-fluorobenzyl chloride solidifies from the liquid state to the solid state, the arrangement of molecules tends to be ordered from disorder, and the lattice structure gradually forms.
The density of 4-fluorobenzyl chloride is about 1.195g/cm ³, which is heavier than water. Placed in water, it sinks to the bottom of the water. This characteristic can be used for discrimination and operation in the separation of mixtures and related experiments and production processes.
In terms of solubility, 4-fluorobenzyl chloride is insoluble in water, but soluble in many organic solvents, such as ethanol, ether, acetone, etc. The difference in solubility is due to the characteristics of its molecular structure, the interaction between polar and non-polar, and the degree of affinity with different solvents. In the field of organic synthesis, this solubility can be used to select a suitable reaction medium to facilitate the reaction.
In addition, the vapor pressure of 4-fluorobenzyl chloride has a fixed value at a specific temperature, and the vapor pressure is related to the difficulty of volatilization. The higher the vapor pressure, under the same conditions, the easier it is to evaporate. When storing and using, it is necessary to pay attention to its volatilization characteristics, and properly seal and store it to prevent volatilization and dissipation, causing component loss, and avoiding harm to the environment and human body.
In summary, the physical properties of 4-fluorobenzyl chloride are of great significance in chemical production, organic synthesis and related scientific research activities, and it is impossible to ignore them.
What are the chemical properties of 4-Fluorobenzyl chloride?
4-Fluorobenzyl chloride, its chemical properties are as follows: This substance has active chemical properties and is widely used in the field of organic synthesis.
In its structure, benzyl is connected to chlorine atoms, and chlorine atoms are highly active, which is prone to nucleophilic substitution. This reaction is due to the strong electronegativity of chlorine atoms, and the carbon-chlorine bond connected to benzyl is vulnerable to attack by nucleophiles, and then the bond is broken. Nucleophiles such as alkoxides, amines or carboxylates can undergo nucleophilic substitution with 4-fluorobenzyl chloride to generate corresponding ethers, amines or esters.
In addition, the presence of 4-fluorobenzyl chloride also affects the reactivity due to the presence of fluorine atoms. Fluorine atoms have a strong electron-absorbing effect. Although the electron cloud density of benzyl groups is reduced, it also enhances the polarity of carbon-chlorine bonds, which to some extent makes nucleophilic substitution reactions easier.
And because of the presence of benzene rings in its structure, 4-fluorobenzyl chloride can also participate in aromatic ring-related reactions. For example, under appropriate conditions, a Fourier-gram reaction can occur, introducing other substituents on the benzene ring, thereby constructing more complex organic molecular structures. However, 4-fluorobenzyl chloride also has drawbacks. Due to its toxicity and irritation, it must be handled with caution and properly disposed of in a well-ventilated environment to prevent harm to personal safety and the environment.
What are the synthesis methods of 4-Fluorobenzyl chloride?
There are several methods for synthesizing 4-fluorobenzyl chloride.
First, 4-fluorotoluene is used as the starting material. Under light conditions, 4-fluorotoluene undergoes a radical substitution reaction with chlorine. In this reaction, chlorine gas generates chlorine radicals under light excitation, which attack the benzyl position hydrogen atom of 4-fluorotoluene, thereby generating 4-fluorobenzyl chloride. During the reaction, attention should be paid to controlling the reaction temperature, chlorine gas penetration rate and light intensity. If the temperature is too high, it is easy to cause polychlorination side reactions; if the chlorine gas is introduced too quickly, it will also lead to an increase in by-products; if the light intensity is not suitable, the reaction rate may be affected.
Second, it can be prepared by the reaction of 4-fluorobenzyl alcohol with chlorination reagents. Commonly used chlorination reagents such as sulfoxide chloride (SOCl ²), phosphorus trichloride (PCl 😉), etc. Taking thionyl chloride as an example, when 4-fluorobenzyl alcohol reacts with thionyl chloride, 4-fluorobenzyl chloride, sulfur dioxide and hydrogen chloride gas are generated. This reaction is usually carried out in suitable organic solvents, such as pyridine. Pyridine can play a role in catalysis and absorption to generate hydrogen chloride gas, and promote the reaction to generate products. During the reaction process, the reaction time and temperature should be controlled. If the reaction time is too short or incomplete, if the temperature is not appropriate, side reactions may occur.
Third, 4-fluorobenzoic acid is used as the starting material. First, 4-fluorobenzoic acid is reduced to 4-fluorobenzyl alcohol, and strong reducing agents such as lithium aluminum hydride (LiAlH) can be selected. Then 4-fluorobenzyl alcohol is converted into 4-fluorobenzyl chloride according to the above method of reacting with chlorination reagents. This path has a little more steps, but the raw material 4-fluorobenzoic acid is more common and relatively easy to obtain. During the operation, when using reducing agents such as lithium aluminum hydride, it needs to be carried out strictly in an anhydrous and oxygen-free environment, because it reacts violently in contact with water, which poses a safety hazard. < Br >
When synthesizing 4-fluorobenzyl chloride, no matter what method is used, many factors such as raw material cost, reaction conditions, yield and product purity need to be comprehensively considered to find the most suitable synthesis path.
What are the precautions for 4-Fluorobenzyl chloride in storage and transportation?
4-Fluorobenzyl chloride is also an organic compound. During storage and transportation, many matters must be paid attention to.
First word storage. This substance is dangerous and should be stored in a cool and ventilated warehouse. If it is in a high temperature environment, it may cause dangerous reactions. The temperature of the warehouse must be strictly controlled and not too high to prevent it from being decomposed by heat or causing other accidents. And it should be kept away from fires and heat sources. Open flames are close, and disasters are easy to occur. It should be stored separately from oxidants and alkalis, and must not be mixed, otherwise it may cause violent chemical reactions and endanger safety. The storage area must also be equipped with suitable materials to contain leaks, in case of leakage, and can be properly handled in time.
Times and transportation. Before transportation, make sure that the packaging is complete and well sealed. If the packaging is damaged, the risk of leakage during transportation will increase greatly. During transportation, the selected vehicles must be equipped with corresponding safety facilities and protective equipment to deal with emergencies. The transportation process must be smooth and avoid bumps and vibrations, otherwise the packaging may be damaged. At the same time, the transportation personnel should also be familiar with its nature and emergency treatment methods, and in case of leakage, they can deal with it quickly and correctly. Do not mix with contraband items, strictly follow the norms and requirements of transportation to ensure the safety of the whole transportation process. In this way, 4-fluorobenzyl chloride can be stored and transported to minimize risks and ensure the safety of personnel and the environment.