Borane;tetrahydrofuran → 2-Bromo-5-(trifluoromethyl)benzyl alcohol

HRID 2075013Notes

Reaction equation

HRID 2075013 reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][C:3]=1[C:4](O)=[O:5].B.O1CCCC1>C1COCC1>[Br:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]([F:13])([F:14])[F:12])=[CH:7][C:3]=1[CH2:4][OH:5]

Participants

4

Procedure

To an ice-cooled solution of 2-bromo-5-(trifluoromethyl)benzoic acid (5.16 g, 19 mmol) in THF (50 mL) was added borane-tetrahydrofuran complex (70 mL of 1M solution in THF, 70 mmol). The resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was quenched with methanol. Solvent was removed. The residue was partitioned between ethyl acetate (3×40 mL) and 1M sodium bicarbonate (50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4) and concentrated to yield the title compound as an oil (4.85 g). 1H NMR (400 MHz, CDCl3) δ 4.8 (s, 2H) 7.5 (m, 1H) 7.7 (d, J=8.2 Hz, 1H) 7.8 (d, J=1.6 Hz, 1H).

Workup

  1. customThe reaction mixture was quenched with methanol
  2. customSolvent was removed
  3. customThe residue was partitioned between ethyl acetate (3×40 mL) and 1M sodium bicarbonate (50 mL)
  4. washThe combined organic layers were washed with saturated NaCl (50 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-287973eb140740d4a81d1eac1c07cb30
Source dataset
uspto-grants-2011_04
Patent number
US07919506B2

Reaction notes

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