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(3-BROMO-4-CHLORO-PHENYL)-METHANOL

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(3-BROMO-4-CHLORO-PHENYL)-METHANOL Basic information

Product Name:
(3-BROMO-4-CHLORO-PHENYL)-METHANOL
Synonyms:
  • (3-BROMO-4-CHLORO-PHENYL)-METHANOL
  • 3-Bromo-4-chlorobenzyl alcohol
  • 3-Bromo-4-chlorobenzenemethanol
  • (3-Bromo-4-chlorophenyl)
  • 3-Bromo-4-chlorobenzyl alcohol 97%
  • Benzenemethanol, 3-bromo-4-chloro-
CAS:
329218-12-4
MF:
C7H6BrClO
MW:
221.48
Mol File:
Mol File
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(3-BROMO-4-CHLORO-PHENYL)-METHANOL Chemical Properties

Boiling point:
307.0±27.0 °C(Predicted)
Density 
1.685
storage temp. 
Sealed in dry,Room Temperature
pka
13.89±0.10(Predicted)
form 
solid
color 
Off White
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Safety Information

HS Code 
2906290090
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(3-BROMO-4-CHLORO-PHENYL)-METHANOL Usage And Synthesis

Synthesis

42860-10-6

329218-12-4

General procedure for the synthesis of 3-bromo-4-chlorobenzyl alcohol from 3-bromo-4-chlorobenzoic acid: A. To a mixture of 3-bromo-4-chlorobenzoic acid (10.0 g, 42.5 mmol) in THF (50 mL) was slowly added 1.0 M borane-THF solution (55.3 mL, 55.3 mmol) under nitrogen protection and at 0 °C. The reaction mixture was stirred overnight at room temperature and then carefully poured into a mixture of NaHCO3/H2O/ice and extracted with EtOAc. The organic layer was washed with saturated aqueous NaCl, dried over MgSO4, filtered and concentrated under reduced pressure to afford the target product 3-bromo-4-chlorobenzyl alcohol (9.4 g, 100%) as a clear, colorless oil.1H NMR (300 MHz, CDCl3) δ 7.61 (s, 1H), 7.41 (d, J = 5.1 Hz, 1H), 7.21 (d, J = 5.1 Hz, 1H), 4.63 (s, 2H), 2.12 (br s, 1H).

References

[1] Patent: WO2011/79102, 2011, A1. Location in patent: Page/Page column 132
[2] Synlett, 2014, vol. 25, # 1, p. 123 - 127
[3] Patent: WO2013/142396, 2013, A1. Location in patent: Page/Page column 55
[4] Patent: US2006/154915, 2006, A1. Location in patent: Page/Page column 29
[5] Patent: WO2003/99776, 2003, A1. Location in patent: Page 63

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