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

HRID 1988535Notes

Reaction equation

HRID 1988535 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

Participants

4

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 room 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, 42.5 mmol, 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-420e9770288c42f790f133b1501725d9
Source dataset
uspto-grants-2010_01
Patent number
US07642220B2

Reaction notes

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