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

HRID 390737

반응식

HRID 390737 반응식
[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]

참가 물질

4

실험 절차

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, 2 H) 7.5 (m, 1 H) 7.7 (d, J=8.2 Hz, 1 H) 7.8 (d, J=1.6 Hz, 1 H).

후처리

  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

출처 및 근거

ORD 기록
ord-0ba15b80095a49f089ecf99eacfd814e
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08383660B2

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