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4-Fluoro-2-(trifluoromethyl)benzyl bromide

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4-Fluoro-2-(trifluoromethyl)benzyl bromide Basic information
Uses
Product Name:4-Fluoro-2-(trifluoromethyl)benzyl bromide
Synonyms:4-FLUORO-2-(TRIFLUOROMETHYL)BENZYL BROMIDE;ALPHA-BROMO-2-FLUORO-4-(TRIFLUOROMETHYL)TOLUENE;ALPHA-BROMO-4-FLUORO-2-(TRIFLUOROMETHYL)TOLUENE;2-FLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE;1-(BROMOMETHYL)-4-FLUORO-2-(TRIFLUOROMETHYL)BENZENE;a-Bromo-4-fluoro-2-(trifluoromethyl)toluene;4-Fluoro-2-(trifluoromethyl)benzyl bromide, 97+%;à-bromo-4-fluoro-2-(trifluoromethyl)toluene
CAS:206860-48-2
MF:C8H5BrF4
MW:257.02
EINECS:625-261-3
Product Categories:Aromatic Halides (substituted);Aryl;Building Blocks;C8;Chemical Synthesis;Fluorinated Building Blocks;Halogenated Hydrocarbons;Organic Building Blocks;Organic Fluorinated Building Blocks;Trifluoromethyl;Fluoro-contained benzyl bromide series
Mol File:206860-48-2.mol
4-Fluoro-2-(trifluoromethyl)benzyl bromide Structure
4-Fluoro-2-(trifluoromethyl)benzyl bromide Chemical Properties
Boiling point 141 °C(lit.)
density 1.665 g/mL at 25 °C(lit.)
refractive index n20/D 1.482(lit.)
Fp 185 °F
form Liquid
Specific Gravity1.665
color Clear colorless to pale yellow
Sensitive Lachrymatory
CAS DataBase Reference206860-48-2(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-27-36/37/39-45
RIDADR UN 2927 6.1/PG 2
WGK Germany 3
Hazard Note Corrosive/Lachrymatory
HazardClass 8
PackingGroup III
HS Code 29039990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4-Fluoro-2-(trifluoromethyl)benzyl bromide Usage And Synthesis
Uses4-Fluoro-2-(trifluoromethyl)benzyl bromide is a hydrocarbon halide that can be used as a pharmaceutical and chemical intermediate.
Chemical Properties4-Fluoro-2-(trifluoromethyl)benzyl bromide is a colorless liquid with a density of 1.665 g/mL at 25 °C (lit.) and a boiling point of 141 °C (lit.).
SynthesisAdd 4-fluoro-2-(trifluoromethyl)benzenemethanol, tribromooxyphosphine and liquid bromine to a 100 mL three-necked flask equipped with an off-gas absorption device, a reflux condenser tube and a thermometer, and stir for 20 min at ambient temperature, and then heat the reaction system to 80 , and follow the thin-layer chromatography, and add a certain amount of saturated aqueous sodium bisulphite after the substrate has been completely involved in the reaction (about 1 h), and then wash out the unreacted liquid bromine. Then the upper layer of aqueous hydrogen bromide solution was separated. The organic phase was dried with anhydrous sodium sulfate and concentrated to obtain the crude product, which was eluted by the eluent of column chromatography purification (ethyl acetate: petroleum ether=1:20) and concentrated to obtain the colorless liquid 4-fluoro-2-(trifluoromethyl)benzyl bromide.
4-Fluoro-2-(trifluoromethyl)benzyl bromide Preparation Products And Raw materials
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