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3-BROMO-5-FLUOROBENZYL ALCOHOL

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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)Methanol
  • (3-Bromo-5-fluorophenyl)
  • Benzenemethanol, 3-bromo-5-fluoro-
  • 3-BROMO-5-FLUOROBENZYL ALCOHOL ISO 9001:2015 REACH
CAS:
216755-56-5
MF:
C7H6BrFO
MW:
205.02
Product Categories:
  • Alcohol
  • Alcohols
  • Bromine Compounds
  • Fluorine Compounds
Mol File:
216755-56-5.mol
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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
pka
13.94±0.10(Predicted)
form 
Liquid
color 
Colorless
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
Hazard Note 
Irritant
HS Code 
2906290090
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3-BROMO-5-FLUOROBENZYL ALCOHOL Usage And Synthesis

Synthesis

176548-70-2

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

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