4-(Bromomethyl)benzoic acid → 4-(Bromomethyl)benzyl alcohol

HRID 2255568Notes

Reaction equation

HRID 2255568 reaction equation
[Br:1][CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](O)=[O:8])=[CH:5][CH:4]=1.B.C1COCC1>C1COCC1>[Br:1][CH2:2][C:3]1[CH:11]=[CH:10][C:6]([CH2:7][OH:8])=[CH:5][CH:4]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

A suspension of 4-bromomethylbenzoic acid (5.04 g, 23.3 mmol) in THF (30 mL) was cooled to 0° C. and treated with borane/THF (35 mmol). The ice bath was removed and the mixture was allowed to warm to room temperature and stirred for 1.5 hours. The excess borane was quenched first with MeOH, then with water. The reaction mixture was then concentrated in vacuo and redissolved in ethyl acetate. The ethyl acetate layer was washed with 5% HCl, water, NaHCO3, brine, dried (MgSO4), filtered, and evaporated in vacuo to afford 4.44 g (94%) of the titled product.

Workup

  1. customThe ice bath was removed
  2. temperatureto warm to room temperature
  3. customThe excess borane was quenched first with MeOH
  4. concentrationThe reaction mixture was then concentrated in vacuo
  5. dissolutionredissolved in ethyl acetate
  6. washThe ethyl acetate layer was washed with 5% HCl, water, NaHCO3, brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customevaporated in vacuo

Sources & evidence

ORD record
ord-baceb28affa84db0859bb75cfe361e3d
Source dataset
uspto-grants-1993_08
Patent number
US05240938

Reaction notes

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