3 Chloro 2 Fluorobenzylcyanide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-Chloro-2-fluorobenzylcyanide
Chemical Formula C8H5ClFN
Molecular Weight 169.58
Appearance Typically a colorless to pale - yellow liquid
Solubility In Water Low solubility in water
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, ethyl acetate
Odor Possibly has a pungent or characteristic odor
Chemical Formula C8H5ClFN
Molar Mass 171.58 g/mol
Appearance Typically a liquid
Solubility In Water Low solubility, likely insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Stability Stable under normal conditions but may react with strong oxidizing agents
Hazard Class Toxic, harmful if swallowed, inhaled or in contact with skin
FAQ

What is the chemistry of 3-Chloro-2-fluorobenzylcyanide?

3-Chloro-2-fluorobenzyl cyanide is a kind of organic compound. Looking at its chemical properties, its reactivity is first discussed. In this compound, both chlorine atoms and fluorine atoms are quite electronegative, which causes the electron cloud density of the benzene ring to change. In the nucleophilic substitution reaction, the benzyl part connected to the chlorine atom and the cyano group is easily attacked by nucleophiles. In case of nucleophiles such as hydroxyl negative ions, chlorine atoms may be replaced by hydroxyl groups to form corresponding hydroxyl-containing derivatives.

Furthermore, due to the existence of cyanyl groups, this compound can undergo many specific reactions. Cyanyl groups can be hydrolyzed, and under acidic or basic conditions, they are gradually converted into carboxyl groups, first into amide intermediates, and then hydrolyzed into carboxylic acids. The hydrolysis rate under alkaline conditions may be faster than that under acidic conditions.

And because it contains halogen atoms, it can participate in metal-catalyzed coupling reactions. For example, under palladium catalysis, it can cross-couple with other organic halides or alkenyl halides to expand carbon chains and build more complex organic structures.

Its physical properties cannot be ignored. Generally speaking, this compound is either liquid or solid at room temperature and has a certain melting boiling point. Due to the existence of polar groups in the molecule, it is slightly soluble in water, but more soluble in common organic solvents such as ethanol, ether, dichloromethane, etc. This property is extremely critical in its separation, purification and reaction operations. < Br >
and its chemical properties are significantly affected by the position and properties of the substituents on the benzene ring. Chlorine and fluorine are in the ortho position, and the electronic effects of the two are superimposed, which makes the activity of the benzene ring show a unique law. It is also necessary for organic synthesis chemists to consider when designing reaction routes and obtaining target products.

What are the main uses of 3-Chloro-2-fluorobenzylcyanide?

3-Chloro-2-fluorobenzyl cyanide has a wide range of uses. In the field of pharmaceutical synthesis, it is often used as a key intermediate. Taking the creation of specific antimalarial drugs as an example, with the help of the unique chemical structure of 3-chloro-2-fluorobenzyl cyanide, it can be converted into substances with specific pharmacological activities through delicate chemical reactions, achieving the effect of anti-malarial parasites.

It also plays an important role in the field of pesticide research and development. The preparation of many new insecticides relies on it as a starting material. Through chemical modification and transformation, insecticides with high toxicity to pests and relatively friendly to the environment can be obtained. Due to its chemical properties, it can precisely act on specific physiological targets of pests, effectively exterminating insects while reducing the impact on non-target organisms.

In addition, in the field of materials science, 3-chloro-2-fluorobenzyl cyanide is also used. The synthesis of some high-performance polymer materials, the introduction of its structural units, can endow the materials with special properties such as excellent thermal stability and chemical stability. This lays the foundation for the preparation of high-end engineering plastics, special coating materials, etc., to meet the strict performance requirements of materials in aerospace, electronics and electrical appliances.

What are 3-Chloro-2-fluorobenzylcyanide synthesis methods?

There are several methods for the synthesis of 3-chloro-2-fluorobenzyl cyanide.

First, it can be started from 3-chloro-2-fluorobenzyl halide. First, take an appropriate amount of 3-chloro-2-fluorobenzyl halide, such as 3-chloro-2-fluorobenzyl chloride or bromide, place it in a reactor, add a cyanide reagent, usually sodium cyanide or potassium cyanide, and dissolve it in a suitable organic solvent, such as N, N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO). Under suitable temperature and stirring conditions, the halogen atom in the halide undergoes nucleophilic substitution reaction with the cyanyl group, the halogen leaves, and the cyanyl group enters to form 3-chloro-2-fluorobenzyl cyanide. This reaction condition is relatively mild and convenient to operate. However, it is necessary to pay attention to cyanide toxicity. Strict safety procedures should be followed during operation.

Second, 3-chloro-2-fluorobenzoic acid is used as raw material. First, 3-chloro-2-fluorobenzoic acid is converted into its acid chloride form, which can be achieved by reacting with sulfoxide chloride or oxalyl chloride. The resulting acid chloride reacts with ammonia to form 3-chloro-2-fluorobenzamide. Afterwards, 3-chloro-2-fluorobenzamide is treated with a dehydrating agent, such as phosphorus pentoxide or phosphorus oxychloride, so that it undergoes a dehydration reaction, and the amide group is converted to a cyano group, thereby obtaining the target product 3-chloro-2-fluorobenzyl cyanide. This path step is slightly complicated, but the raw materials are more common, and the reaction conditions of each step can be controlled.

Third, start from 3-chloro-2-fluorobenzaldehyde. First, 3-chloro-2-fluorobenzaldehyde is cyanohydrated with sodium cyanide or potassium cyanide under alkaline conditions to generate 3-chloro-2-fluoro - α - hydroxyl benzyl cyanide. Then, through dehydration, the hydroxyl group and adjacent hydrogen atoms are removed to form a carbon-carbon double bond, and then 3-chloro-2-fluorobenzyl cyanide is obtained. This process requires precise control of the reaction conditions, especially the alkaline strength and dehydration conditions, to ensure the purity and yield of the product.

The synthesis of 3-chloro-2-fluorobenzyl cyanide has various methods, each with its own advantages and disadvantages. In practical application, the appropriate synthesis path should be carefully selected according to factors such as the availability of raw materials, reaction conditions and target product requirements.

3-Chloro-2-fluorobenzylcyanide need to pay attention to when storing and transporting

3-Chloro-2-fluorobenzyl cyanide is a special chemical substance, and many things must be paid attention to when storing and transporting it.

Bear the brunt, and choose a cool, dry and well-ventilated place for storage. This chemical substance is susceptible to moisture and high temperature, causing quality deterioration, and even triggering dangerous reactions. High temperature can increase its volatilization rate, causing an increase in concentration in the air, especially dangerous in confined spaces, or causing disasters such as explosions; humid environment may cause reactions such as hydrolysis, which damage its chemical structure and properties.

Second, the choice of storage container is also crucial. Use a corrosion-resistant, well-sealed container to prevent leakage. Because the substance is toxic and corrosive, once it leaks, it will not only damage the environment, but also endanger the safety of surrounding personnel. Containers made of commonly used glass or specific plastics should be carefully selected according to their chemical characteristics to ensure that they do not react chemically.

Furthermore, when transporting, it is necessary to operate in strict accordance with relevant regulations and standards. Packaging should be stable, and buffer materials should be sufficient to prevent damage to the container caused by collision and vibration. Transportation vehicles must be equipped with corresponding emergency response equipment and protective equipment to prepare for emergencies. Transportation personnel should also be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods.

In addition, prominent warning signs should be set up in storage and transportation areas to indicate the danger of the substance and prevent unrelated personnel from approaching. And it is necessary to establish a sound management and monitoring mechanism to regularly check the condition of the container and environmental parameters to ensure the safety of the storage and transportation process. A little carelessness may lead to serious consequences, endangering life, property and the ecological environment.

3-Chloro-2-fluorobenzylcyanide impact on the environment and human health

3-Chloro-2-fluorobenzyl cyanide is an organic compound that is occasionally used in the field of industrial synthesis. However, this substance has latent risks to the environment and human health.

First, the impact on the environment. If it is accidentally released into the environment, in the water body, or due to its relatively stable chemical properties, it is difficult to decompose in time, and then cause water pollution. If aquatic organisms are exposed to water bodies containing this substance for a long time, it may cause physiological disorders. For example, fish may have abnormal respiration and reproduction. In the long run, it may reduce the number of aquatic organisms and destroy the balance of aquatic ecosystems. In the soil, the substance may be adsorbed on soil particles, affecting the normal activities of soil microorganisms, thereby interfering with the nutrient circulation and material transformation process in the soil, reducing soil fertility and affecting plant growth.

Re-discussion on the impact on human health. Inhaled through the respiratory tract, this substance may irritate the mucosa of the respiratory tract, causing uncomfortable symptoms such as cough and asthma. If the inhalation amount is large, or involves the lungs, it will affect gas exchange and cause breathing difficulties in severe cases. After skin contact, it may enter the human body through the skin barrier, causing skin allergies, redness, swelling, itching and other conditions. Long-term exposure or damage to the stratum corneum of the skin, reducing skin defense function. If accidentally ingested, in the gastrointestinal tract, the substance may react with biomolecules in the body, corroding the gastrointestinal mucosa, causing nausea, vomiting, abdominal pain, diarrhea and other toxic symptoms. More seriously, this substance may affect the human nervous system, interfere with the transmission of neurotransmitters, and cause dizziness, headache, fatigue, insomnia, etc. Long-term exposure may even cause irreversible damage to the nervous system.

Therefore, when producing and using products containing 3-chloro-2-fluorobenzyl cyanide, it is necessary to strictly follow the safety operating procedures and strengthen protective measures to prevent it from harming the environment and human health.