Chemical Formula | C7H5Br2F |
Molar Mass | 269.92 g/mol |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Data may vary, around 250 - 270 °C (approximate) |
Density | Approximately 2.0 - 2.2 g/cm³ (estimated) |
Solubility | Slightly soluble in water, soluble in common organic solvents like dichloromethane, chloroform |
Flash Point | Relatively high, as it is an organic halide (approx. >100 °C) |
Hazard Class | Corrosive and toxic due to bromine and fluorine content |
Stability | Stable under normal conditions, but can react with strong bases, oxidizing agents |
Name | 3 - bromo - 5 - fluorobenzyl bromide |
Molecular Formula | C7H5Br2F |
Molecular Weight | 269.92 |
Appearance | Typically a colorless to light - colored liquid or solid (physical state may depend on conditions) |
Boiling Point | Estimated to be in a certain range based on similar compounds, around 230 - 250°C (approximate, actual value may vary) |
Density | Density would be greater than water, around 2.0 - 2.2 g/cm³ (approximate) |
Solubility | Insoluble in water, soluble in organic solvents like dichloromethane, chloroform |
Flash Point | May have a flash point in a flammable range, perhaps around 100 - 120°C (approximate) |
Hazard | Corrosive, harmful if swallowed, inhaled or in contact with skin, may cause burns |
3-bromo-5-fluorobenzyl chemical properties of bromide
3-Bromo-5-fluorobenzyl bromide is an organic compound with active properties, typical of halogenated hydrocarbons. This substance contains two halogen atoms of bromine and fluorine, and there are also bromine atoms at the benzyl position.
Let's talk about its nucleophilic substitution reaction first. Because halogen atoms have nucleophilic substitution activity, they are easy to react when encountering nucleophilic reagents. If reacted with sodium alcohol, halogen atoms can be replaced by alkoxy groups to obtain corresponding ethers. Reacted with ammonia or amine, halogen atoms will be replaced by amino groups to obtain nitrogen-containing derivatives. Under basic conditions, when reacted with water, halogen atoms can be replaced by hydroxyl groups to produce corresponding alcohols.
And then its elimination reaction. Under the action of a strong base, this compound can undergo elimination reactions. If co-heated with potassium alcohol, the bromine atom at the benzyl position and the hydrogen atom at the ortho position can remove hydrogen bromide and form a carbon-carbon double bond to obtain a product containing an alkene bond.
It also has the characteristics of a halogen atom. Bromine atoms can participate in the conversion related to bromination reactions, while fluorine atoms are relatively stable, but under certain conditions, they can also participate in reactions such as nucleophilic fluorination.
In addition, this compound has a certain polarity due to the halogen atom, and has a certain solubility in organic solvents. However, its solubility is also affected by the molecular structure and solvent properties. < Br >
In the field of organic synthesis, 3-bromo-5-fluorobenzyl bromide is often used as an important intermediate. Through its nucleophilic substitution, elimination and other reactions, a variety of organic molecular structures can be constructed for the preparation of drugs, pesticides and functional materials.
What are the main uses of 3-bromo-5-fluorobenzyl bromide?
3-Bromo-5-fluorobenzyl bromide is a commonly used chemical reagent in the field of organic synthesis, and its use is quite extensive.
First, in the field of medicinal chemistry, it is often used as a key intermediate. The construction of many drug molecules requires the introduction of specific functional groups through its unique structure. Because its structure contains bromine and fluorine atoms, it can participate in a variety of organic reactions, such as nucleophilic substitution reactions. Drug developers can use this reaction to connect other biologically active groups to synthesize compounds with specific pharmacological activities, laying the foundation for the creation of new drugs.
Second, in the field of materials science, it also has important uses. Through chemical reactions, it can be introduced into the structure of polymer materials. The properties of bromine and fluorine atoms can change the physical and chemical properties of materials, such as improving the flame retardancy of materials. The introduction of fluorine atoms may also enhance the chemical resistance and thermal stability of materials, making materials suitable for more special environments, such as aerospace, electronic devices and other fields that require strict material properties.
Third, in organic synthesis chemistry, it is an important synthetic building block. Chemists can use it to carry out a series of complex organic synthesis reactions to construct organic molecules with specific structures and functions. By selecting different reaction conditions and reagents, the molecular structure can be precisely regulated, and organic compounds with novel structures and properties can be synthesized, promoting the development of organic synthesis chemistry. With its unique structure, 3-bromo-5-fluorobenzyl bromide plays an indispensable role in many fields such as medicinal chemistry, materials science and organic synthetic chemistry, providing an important material basis for innovation and development in various fields.
What is the synthesis method of 3-bromo-5-fluorobenzyl bromide?
The synthesis of 3-bromo-5-fluorobenzyl bromide is an important topic in organic synthetic chemistry. There are many synthesis paths, which can vary according to different starting materials and reaction conditions.
Common synthesis methods can be started from 3-bromo-5-fluorotoluene. First, in the presence of a suitable brominating agent, such as N-bromosuccinimide (NBS), in the presence of an initiator such as benzoyl peroxide (BPO), in a suitable solvent such as carbon tetrachloride, the radical substitution reaction is carried out by heating and refluxing. In this reaction, NBS provides bromine free radicals to attack the hydrogen atom at the benzyl position to generate 3-bromo-5-fluorobenzyl bromide.
Or from 3-bromo-5-fluorobenzoic acid, it can be reduced to 3-bromo-5-fluorobenzyl alcohol first, and the commonly used reducing agent is lithium aluminum hydride (LiAlH). Then, 3-bromo-5-fluorobenzyl alcohol is treated with hydrobromic acid or phosphorus tribromide (PBr). After substitution, the hydroxyl group is replaced with a bromine atom to obtain 3-bromo-5-fluorobenzyl bromide.
Another way of thinking is to start with 3-bromo-5-fluorobenzaldehyde, first reduce 3-bromo-5-fluorobenzyl alcohol, and then react with the previous method to obtain the target product by halogenation.
During the synthesis process, attention should be paid to the precise control of reaction conditions, such as temperature, reaction time, and reagent dosage, which all have a great impact on the reaction yield and selectivity. At the same time, the separation and purification of the product is also crucial. Commonly used methods include column chromatography and recrystallization to obtain high-purity 3-bromo-5-fluorobenzyl bromide.
What are the precautions for 3-bromo-5-fluorobenzyl bromide in storage and transportation?
3-Bromo-5-fluorobenzyl bromide is also an organic compound. During storage and transportation, many matters must not be ignored.
First words storage, this compound has a certain chemical activity and should be stored in a cool, dry and well ventilated place. Due to heat and humidity, it is easy to cause deterioration or cause chemical reactions. If placed in a high temperature place, it may cause decomposition, damage its quality, and may cause dangerous side reactions. Therefore, the warehouse temperature should be controlled within a suitable range, such as between 5 ° C and 25 ° C, and the humidity should not be too high. It is appropriate to maintain it at 40% - 60%.
Furthermore, it is necessary to avoid contact with oxidants, strong bases and other substances. When the cover 3-bromo-5-fluorobenzyl bromide encounters an oxidant, it is prone to oxidation reaction; when it encounters a strong alkali, there may be reactions such as hydrolysis, which can cause changes in the structure and properties of the compound. When storing, it must be stored separately and at a safe distance from the above items.
As for transportation, because it may be toxic and corrosive, during transportation, protective measures must be comprehensive. The packaging should be solid and reliable to prevent leakage. The packaging materials used should be resistant to the erosion of this compound. When loading and unloading, the operation should be careful not to damage the packaging.
In the transportation vehicle, a suitable environment should also be maintained, and it should not be overheated or damp. And transportation personnel must be professionally trained to be familiar with the characteristics of this compound and emergency treatment methods. If a leak occurs during transportation, effective measures should be taken immediately, such as evacuating the crowd, preventing the spread of pollution, and using suitable materials to absorb or neutralize the leak to ensure environmental and personal safety.
What is the market price range for 3-bromo-5-fluorobenzyl bromide?
3-Bromo-5-fluorobenzyl bromide is an important compound in organic chemistry. Its market price range is difficult to determine, because it is affected by many factors.
First, the cost of raw materials has a great impact on the price of this compound. If the starting material required for synthesis is rare, or its price fluctuates due to season, origin, supply and demand, the price of 3-bromo-5-fluorobenzyl bromide will also fluctuate. Second, the simplicity and cost of the preparation process are also critical. Complex and high-cost synthesis methods require special catalysts and harsh reaction conditions, which will increase their price; simple and efficient processes may reduce costs and prices.
Furthermore, the state of market supply and demand is also the main factor in determining the price. If the demand for this compound in the pharmaceutical, materials and other industries increases sharply, but the supply is limited, the price will rise; if the demand is low and the supply is excessive, the price may decline.
Looking at past market conditions, the price of such fine chemicals often fluctuates. In some specific periods and specific market areas, the price per gram may range from tens to hundreds of yuan. However, this is only a rough number, and it is difficult to determine with the rapid changes in the market. Therefore, in order to know the exact market price range, it is necessary to research the chemical product trading platform in real time and consult the industry suppliers in order to obtain a more accurate price.