3 Bromo 2 Chlorobenzotrifluoride
Fluoride
3-Bromo-2-chlorobenzotrifluoride
Chemical Formula C7H3BrClF3
Molecular Weight 261.45
Appearance Liquid (usually)
Boiling Point Data needed
Melting Point Data needed
Density Data needed
Solubility In Water Low (expected, due to non - polar nature)
Solubility In Organic Solvents Good solubility in common organic solvents like dichloromethane, toluene
Vapor Pressure Data needed
Flash Point Data needed
Refractive Index Data needed
FAQ

What is the chemistry of 3-Bromo-2-chlorobenzotrifluoride?

3-Bromo-2-chlorotrifluorotoluene is an organic compound. Its physical properties are colorless to light yellow liquid at room temperature, with a special odor, insoluble in water, soluble in most organic solvents, such as ethanol, ether, benzene, etc. Due to the molecular structure containing trifluoromethyl, it has high hydrophobicity.

Discussing the chemical properties, first, the characteristics of halogenated aromatics are significant. Bromine and chlorine atoms are highly active and can participate in many nucleophilic substitution reactions. For example, under basic conditions, hydroxyl negative ions can attack the carbon atoms attached to the halogen on the benzene ring, and the halogen atoms leave to form corresponding phenolic derivatives. In this reaction mechanism, the nucleophilic reagent hydroxyl negative ion provides an electron pair to form a new bond with the carbon atom of the benzene ring, and the halogen ion leaves with a pair of electrons.

Second, trifluoromethyl has a significant impact. Trifluoromethyl has strong electron absorption, which reduces the electron cloud density of the benzene ring and increases the difficulty of electrophilic substitution reaction on the benzene ring. Compared with ordinary alkyl-substituted benzene, electrophilic reagents are more difficult to attack the benzene ring. However, under certain conditions, such as the use of strong electrophilic reagents and suitable catalysts, electrophilic substitution can still occur, and the substitution position is affected by the positioning effect of bromine, chlorine and trifluoromethyl.

Third, under reduction conditions, bromine and chlorine atoms in the molecule can be removed by For example, under the action of certain metal catalysts and reducing agents, the dehalogenation reaction can be achieved to generate halogen-free benzene derivatives.

Fourth, the carbon-fluorine bond in this compound is highly stable and difficult to break under normal conditions. However, in the presence of high temperatures, strong oxidants or special catalysts, the carbon-fluorine bond may react, but such reaction conditions are harsh.

In short, 3-bromo-2-chlorotrifluorotoluene can be used as a key intermediate in the field of organic synthesis due to its special structure. It participates in a variety of organic reactions to synthesize organic compounds with different functions.

What are the main uses of 3-Bromo-2-chlorobenzotrifluoride?

3-Bromo-2-chlorotrifluorotoluene is a crucial intermediate in organic synthesis and is widely used in many fields.

First, in the field of medicinal chemistry, it is often the key raw material for the synthesis of specific drugs. Taking some antibacterial drugs as an example, the construction of their molecular structures, 3-bromo-2-chlorotrifluorotoluene can be used as a starting material. Through a series of delicate chemical reactions, such as nucleophilic substitution, coupling reactions, etc., drug molecules with specific biological activities are gradually built. Its unique structure can endow drugs with better fat solubility and stability, thereby enhancing the ability of drugs to penetrate biofilms and improving drug efficacy.

Second, in the field of pesticide chemistry, this compound is also indispensable. It can be used to create new pesticides. By ingenious modification and derivatization of its structure, efficient pesticides for specific pests or diseases can be developed. For example, it can be used as a key intermediate to synthesize insecticides with unique mechanisms of action, interfering with the nervous system or physiological metabolic processes of pests, achieving the purpose of efficient insecticides, and reducing the impact on the environment, in line with the current trend of green pesticide development.

Third, in the field of materials science, 3-bromo-2-chlorotrifluorotoluene also plays an important role. It can be used to synthesize high-performance functional materials, such as fluoropolymers. Introducing it into the polymer structure can significantly improve the properties of the material, such as improving the material's weather resistance, chemical stability, low surface energy and other characteristics. These high-performance materials are widely used in high-end fields such as aerospace, electronics and electrical appliances, and can meet the strict requirements of material properties in special environments.

In summary, 3-bromo-2-chlorotrifluorotoluene has a unique structure and is an extremely important chemical raw material in many fields such as medicine, pesticides, and materials, promoting technological progress and innovation in various fields.

What is 3-Bromo-2-chlorobenzotrifluoride synthesis method?

The preparation of 3-bromo-2-chlorotrifluorotoluene often involves a multi-step reaction. The first step is to use 2-chlorotrifluorotoluene as the starting material. Due to the substituent effect on the aromatic ring, trifluoromethyl is the meta-locator, and the chlorine atom is the o-locator and the para-locator, the two work together to make the reaction check point selective.

First, 2-chlorotrifluorotoluene is reacted with a brominating reagent. Commonly used brominating reagents, such as bromine ($Br_ {2} $), react in the presence of a suitable catalyst. This catalyst is often Lewis acid, such as ferric chloride ($FeCl_ {3} $) or ferric tribromide ($FeBr_ {3} $). The reaction mechanism is electrophilic substitution, and bromine molecules polarize under the action of the catalyst to form active electrophilic reagents and attack aromatic rings. Due to the strong electron-absorbing action of trifluoromethyl, the density of the ortho-and para-electron clouds decreases, and the meta-position is relatively high. Although the chlorine atom is the ortho-and para-position group, the combined effect of steric hindrance and electronic effect makes bromine mainly replace the ortho-position of chlorine to generate 3-bromo-2-chlorotrifluorotoluene.

For specific operation, put 2-chlorotrifluorotoluene into the reaction vessel equipped with a stirrer, thermometer and reflux condenser, add an appropriate amount of catalyst, and slowly drop bromine at low temperature. The reaction process needs to be closely monitored, and the reaction process can be tracked by thin layer chromatography (TLC). After the reaction is completed, the reaction solution is washed with water, alkali washed to remove the unreacted bromine and catalyst, and then dried and distilled to obtain a crude product. The crude product often needs to be further distilled to improve the purity of the product, and finally obtain high-purity 3-bromo-2-chlorotrifluorotoluene. Although this preparation method has clear steps, the control of reaction conditions is crucial, and there are certain requirements for reaction equipment and operation, so as to obtain products with satisfactory yield and purity.

What are the precautions in storage and transportation of 3-Bromo-2-chlorobenzotrifluoride?

3-Bromo-2-chlorotrifluorotoluene is also an organic compound. During storage and transportation, more attention should be paid.

First storage, this compound should be stored in a cool, dry and well-ventilated place. Because of its certain chemical activity, high temperature and humid environment, it is easy to cause deterioration and damage its chemical properties. The temperature of the warehouse should be controlled within a specific range to avoid chemical reactions caused by excessive temperature. And it must be kept away from fire and heat sources. The genus of fireworks is a taboo to prevent the risk of explosion.

Furthermore, it should be stored separately from oxidants and alkalis, and should not be mixed. Due to its chemical properties, it encounters with various substances, or reacts violently, causing safety problems. Where it is stored, suitable containment materials should be prepared to prevent leakage, and it can be handled in time to avoid polluting the environment.

As for transportation, it should not be ignored. Before transportation, make sure that the container is well sealed to prevent its leakage and volatilization. During transportation, the speed should be stable, and do not brake or turn sharply to avoid damage to the container. Transportation vehicles must be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment. Drivers and escorts should be familiar with the properties of this compound and emergency treatment methods. If there is a leak on the way, they can quickly implement effective measures to reduce the damage.

In short, when storing and transporting 3-bromo-2-chlorotrifluorotoluene, all the details are related to safety, and it must be carried out in accordance with regulations to ensure safety.

3-Bromo-2-chlorobenzotrifluoride impact on the environment and people

3-Bromo-2-chlorotrifluorotoluene is also an organic compound. In the environment and human body, its impact is quite well investigated.

First talk about its impact on the environment. If this substance is released in nature, it is difficult to be naturally degraded due to its chemical stability, or it can accumulate in the environment. In the soil, it may hinder the uptake of nutrients by plant roots, causing plant growth to be trapped, stunted, or reduce crop production. Entering the water body will endanger aquatic organisms. Or break its cell membrane, disturb its physiological metabolism, cause abnormal behavior of aquatic organisms, hindered reproduction, and even death, and destroy the ecological balance of water. And because of its volatility, it generates harmful secondary pollutants in the atmosphere or participates in photochemical reactions, which affects air quality and may have potential effects on regional climate.

Re-discuss its impact on the human body. If people inhale through the respiratory tract, contact with the skin or accidentally eat things containing this substance, it can be harmful. Entering the body through the respiratory tract, or irritating the mucosa of the respiratory tract, causing cough, asthma, breathing difficulties and other diseases. Long-term exposure may damage lung function and increase the risk of respiratory diseases. Contact through the skin may cause skin allergies, redness, and itching. If the skin has wounds, it is more likely to penetrate into the body and damage internal organs. After ingestion, or irritate the stomach, causing nausea, vomiting, abdominal pain, diarrhea and other gastrointestinal discomfort. This substance may be potentially carcinogenic, teratogenic, mutagenic, long-term exposure, or damage human genetic material, increase the risk of cancer, in pregnant women, or endanger fetal development, resulting in fetal malformation and other serious consequences.

In short, 3-bromo-2-chlorotrifluorotoluene is potentially harmful to the environment and human body. When it is produced, used and disposed of, strict safety measures should be taken to prevent its release into the environment to protect the ecological environment and human health.