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2-Bromo-4-(trifluoromethyl)phenol

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2-Bromo-4-(trifluoromethyl)phenol manufacturers

2-Bromo-4-(trifluoromethyl)phenol Basic information
Product Name:2-Bromo-4-(trifluoromethyl)phenol
Synonyms:BUTTPARK 180\07-84;3-Bromo-4-hydroxybenzotrifluoride;2-Bromo-4-(trifluoromethyl)phenol, 2-Bromo-alpha,alpha,alpha-trifluoro-p-cresol;2-Bromo-4-(trifluoromethyl)phenol >;Phenol, 2-bromo-4-(trifluoromethyl)-;2-Bromo-4-(trifluoromethyl)phenol
CAS:81107-97-3
MF:C7H4BrF3O
MW:241.01
EINECS:
Product Categories:
Mol File:81107-97-3.mol
2-Bromo-4-(trifluoromethyl)phenol Structure
2-Bromo-4-(trifluoromethyl)phenol Chemical Properties
Boiling point 196.7±35.0 °C(Predicted)
density 1.752±0.06 g/cm3(Predicted)
refractive index 1.4960 to 1.5000
storage temp. Inert atmosphere,Room Temperature
pka7.03±0.18(Predicted)
form Liquid
color Brown
λmax317nm(CH3CN)(lit.)
CAS DataBase Reference81107-97-3
Safety Information
HS Code 2908190090
MSDS Information
2-Bromo-4-(trifluoromethyl)phenol Usage And Synthesis
Chemical PropertiesLight brown liquid
Synthesis
4-Trifluoromethylphenol

402-45-9

2-BROMO-4-(TRIFLUOROMETHYL)PHENOL

81107-97-3

The general procedure for synthesizing 2-bromo-4-trifluoromethylphenol from p-trifluoromethylphenol is as follows: 32 g of p-trifluoromethylphenol was dissolved in 200 mL of dichloromethane. An equimolar amount of bromine was slowly added dropwise under cooling conditions, and the dropwise process lasted about 2 hours. After the dropwise addition was completed, the reaction mixture was continued to be stirred at room temperature for 12 hours. Upon completion of the reaction, the reaction system was washed with saturated sodium bicarbonate solution to neutral. Subsequently, the organic phase was dried and the solvent was removed by distillation to give 40 g of a thick liquid product. This thick liquid is the target compound 2-bromo-4-trifluoromethylphenol.

References[1] Tetrahedron, 2003, vol. 59, # 34, p. 6545 - 6558
[2] Patent: WO2009/89192, 2009, A1. Location in patent: Page/Page column 30-31
[3] Chemistry - A European Journal, 2012, vol. 18, # 11, p. 3286 - 3291
[4] Chemical and Pharmaceutical Bulletin, 1996, vol. 44, # 4, p. 734 - 745
[5] Tetrahedron Letters, 2001, vol. 42, # 45, p. 8093 - 8096
2-Bromo-4-(trifluoromethyl)phenol Preparation Products And Raw materials
Raw materials4-Trifluoromethylphenol-->Dichloromethane
Preparation Products2-Hydroxy-5-trifluoromethylbenzonitrile-->2'-hydroxy-5'-(trifluoroMethyl)acetophenone
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