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3-BROMO-5-FLUOROBENZYL ALCOHOL

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3-BROMO-5-FLUOROBENZYL ALCOHOL manufacturers

3-BROMO-5-FLUOROBENZYL ALCOHOL Basic information
Product Name:3-BROMO-5-FLUOROBENZYL ALCOHOL
Synonyms:3-BROMO-5-FLUOROBENZYL ALCOHOL;3-Bromo-5-fluorobenzyl alcohol 98%;3-Bromo-5-fluorobenzylalcohol98%;(3-Bromo-5-fluorophenyl);Benzenemethanol, 3-bromo-5-fluoro-;3-BROMO-5-FLUOROBENZYL ALCOHOL ISO 9001:2015 REACH;(3-BroMo-5-fluorophenyl)Methanol
CAS:216755-56-5
MF:C7H6BrFO
MW:205.02
EINECS:
Product Categories:Alcohol;Alcohols;Bromine Compounds;Fluorine Compounds
Mol File:216755-56-5.mol
3-BROMO-5-FLUOROBENZYL ALCOHOL Structure
3-BROMO-5-FLUOROBENZYL ALCOHOL Chemical Properties
Boiling point 259.0±25.0 °C(Predicted)
density 1.658±0.06 g/cm3(Predicted)
storage temp. Store at room temperature
pka13.94±0.10(Predicted)
form Liquid
color Colorless
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
Hazard Note Irritant
HS Code 2906290090
MSDS Information
3-BROMO-5-FLUOROBENZYL ALCOHOL Usage And Synthesis
Synthesis
3-Bromo-5-fluorobenzoic acid

176548-70-2

3-BROMO-5-FLUOROBENZYL ALCOHOL

216755-56-5

General procedure for the synthesis of (3-bromo-5-fluorophenyl)methanol from 3-bromo-5-fluorobenzoic acid: 3-bromo-5-fluorobenzoic acid (1.0 g, 4.52 mmol) was suspended in tetrahydrofuran (8 mL) and the mixture was cooled to 0°C. Borane tetrahydrofuran complex (1 M in tetrahydrofuran, 9 mL, 9.0 mmol) was added slowly and dropwise over 15 min. The reaction mixture was gradually warmed to room temperature and stirred overnight. Upon completion of the reaction, the mixture was cooled again to 0 °C and the reaction was quenched by careful addition of excess methanol. Subsequently, the reaction mixture was diluted with ethyl acetate and washed sequentially with 1 N sodium hydroxide solution (2×) and saturated brine (2×). The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 0.88 g (95% yield) of the white solid product (3-bromo-5-fluorophenyl)methanol. The structure of the product was confirmed by 1H-NMR (CDCl3, 500 MHz): δ 7.29 (s, 1H), 7.16 (d, J = 7.9 Hz, 1H), 7.03 (d, J = 9.2 Hz, 1H), 4.66 (s, 2H).

References[1] Patent: US2007/249607, 2007, A1. Location in patent: Page/Page column 81
[2] Patent: CN104447730, 2017, B. Location in patent: Paragraph 0146-0147
[3] Patent: WO2016/54728, 2016, A1. Location in patent: Paragraph 00127
[4] Patent: WO2016/74068, 2016, A1. Location in patent: Paragraph 00121
[5] Patent: WO2006/79791, 2006, A1. Location in patent: Page/Page column 44
3-BROMO-5-FLUOROBENZYL ALCOHOL Preparation Products And Raw materials
Raw materials3-Bromo-5-fluorobenzoic acid-->Tetrahydrofuran-->BORANE THF-->Methanol
Preparation Products3-Bromo-5-fluorophenylacetonitrile
Tag:3-BROMO-5-FLUOROBENZYL ALCOHOL(216755-56-5) Related Product Information
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