Bromo(phenyl)acetic acid → 2-Bromo-2-phenylethanol

HRID 893584Notes

Reaction equation

HRID 893584 reaction equation
[Br:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:3](O)=[O:4].B#B.O1CCCC1.O>O1CCCC1>[Br:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH2:3][OH:4]

Participants

5

Procedure

To a stirred solution of 25 g of alpha-bromophenylacetic acid in 100 ml of dry tetrahydrofuran was added 151 ml of 1.0M diborane in tetrahydrofuran dropwise at 5° C. under argon over 30 minutes. This mixture was stirred overnight at room temperature, then cooled to 0° C. and 130 ml of tetrahydrofuran:water (1:1) was added dropwise. The mixture was then saturated with potassium carbonate and the tetrahydrofuran removed. The aqueous remainder was extracted three times with ether. The extracts were combined and dried. The residue was triturated with hexane and the solid collected giving the desired compound as white needles, mp 38-39° C.

Workup

  1. temperaturecooled to 0° C.
  2. customsaturated with potassium carbonate and the tetrahydrofuran removed
  3. extractionThe aqueous remainder was extracted three times with ether
  4. customdried
  5. customThe residue was triturated with hexane
  6. customthe solid collected

Sources & evidence

ORD record
ord-c8a0dedd703e4093bb9c922a9fc35b22
Source dataset
uspto-grants-1992_06
Patent number
US05126291

Reaction notes

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