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Sodium borohydride → 1-(5-Bromo-2-chlorophenyl)ethanol

HRID 506446
Notes
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Reaction equation

HRID 506446 reaction equation
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[CH:6][C:7]([Cl:13])=[C:8]([C:10](=[O:12])[CH3:11])[CH:9]=1>CO>[Br:3][C:4]1[CH:5]=[CH:6][C:7]([Cl:13])=[C:8]([CH:10]([OH:12])[CH3:11])[CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 136281451-(5-Bromo-2-chlorophenyl)ethan-1-one

Product 1

HCID 587626441-(5-Bromo-2-chlorophenyl)ethanolYield 99.2%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Sodium borohydride (1.182 g, 51.4 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanone (10 g, 42.8 mmol) in methanol at 0° C. The resulting bubbling white mixture was allowed to warm to ambient temperature and stirred for 2 h. The reaction mixture was quenched with acetone (50 mL) and concentrated by rotary evaporation. The residue was partitioned between ethyl acetate and water. The organic phase was dried and concentrated to yield the title compound (10 g, 99% yield) as a white solid: 1H NMR (CDCl3) δ 7.75 (d, 1H), 7.32 (m, 1H), 7.19 (m, 1H), 5.23 (q, 1H), 1.95 (d, 1H), 1.48 (d, 3H).

Workup

  1. customThe resulting bubbling white mixture
  2. customThe reaction mixture was quenched with acetone (50 mL)
  3. concentrationconcentrated by rotary evaporation
  4. customThe residue was partitioned between ethyl acetate and water
  5. customThe organic phase was dried
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-fa53a66b553842db98aa096d79ab48cd
Source dataset
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07786044B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes