4-Chloro-3-(trifluoromethyl)benzyl bromide - Names and Identifiers
4-Chloro-3-(trifluoromethyl)benzyl bromide - Physico-chemical Properties
Molecular Formula | C8H5BrClF3
|
Molar Mass | 273.48 |
Density | 1.663 |
Melting Point | 36-40℃ |
Boling Point | 234℃ |
Flash Point | 95℃ |
Vapor Presure | 0.0831mmHg at 25°C |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | 1.505 |
MDL | MFCD01631540 |
4-Chloro-3-(trifluoromethyl)benzyl bromide - Risk and Safety
Hazard Symbols | C - Corrosive
|
Risk Codes | R34 - Causes burns
R36/37/38 - Irritating to eyes, respiratory system and skin.
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
|
UN IDs | 1760 |
Hazard Class | 8 |
Packing Group | III |
4-Chloro-3-(trifluoromethyl)benzyl bromide - Introduction
4-choro-3-(trifluoromethyl)benzyl bromide is an organic compound with the chemical formula C8H6BrClF3.
Nature:
-Appearance: White crystalline solid
-Melting point: 50-52 ° C
-Boiling Point: 183-184 ° C
-Density: 1.8g/cm³
-Solubility: Soluble in organic solvents such as ethanol and dimethyl sulfoxide, insoluble in water
-the main risk: irritant to the eyes, skin and respiratory system, for irritating substances
Use:
- 4-Chloro-3-(trifluoromethyl)benzyl bromide is commonly used as a reagent in organic synthesis
-can be used as acyl transfer reagent and bromination reagent, commonly used in allylation reaction and substitution reaction
-There are also some applications in the field of pesticides and pharmaceuticals
Method:
4-Chloro-3-(trifluoromethyl)benzyl bromide is generally prepared by the following steps:
1. First, 3-trifluoromethylbenzoic acid is reacted with trimethyl phosphite under alkaline conditions to produce trimethyl 3-(trifluoromethyl) benzoate.
2. Trimethyl 3-(trifluoromethyl) benzoate was then brominated with bromine solution to give trimethyl 4-bromo-3-(trifluoromethyl) benzoate.
3. Finally, trimethyl 4-bromo-3-(trifluoromethyl) benzoate is reduced with hydrogen bromide to produce trimethyl 4-chloro-3-(trifluoromethyl) benzoate. This intermediate is then oxidized with sodium hypochlorite and finally reacted with trifluoroacetic acid and hydrofluoric acid to give the final product, 4-Chloro-3-(trifluoromethyl)benzyl bromide.
Safety Information:
When using 4-Chloro-3-(trifluoromethyl)benzyl bromide, it is necessary to strictly follow the safety procedures, wear protective glasses and gloves, and avoid contact with skin and eyes. Use in a well-ventilated place, avoid inhalation or ingestion. In case of accidental contact or ingestion, the affected area should be cleaned immediately and medical help should be sought.
Last Update:2024-04-09 21:01:54