Boron tribromide → 3-Amino-2-fluorophenol

HRID 631586노트

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HRID 631586 반응식
[F:1][C:2]1[C:8]([O:9]C)=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].B(Br)(Br)Br>ClCCl>[NH2:4][C:3]1[C:2]([F:1])=[C:8]([OH:9])[CH:7]=[CH:6][CH:5]=1

참가 물질

4

실험 절차

To a stirred solution of 2-fluoro-3-methoxyaniline (3.0 g, 21.26 mmol) in dichloromethane (80 mL), at 0° C., was added a 4.0 M solution of boron tribromide in dichloromethane (10.63 mL, 42.52 mmol). The reaction mixture was allowed to warm to rt and stirring was continued for a further 15 h. The reaction mixture was quenched via the addition of methanol. After concentration under reduced pressure, the residue was taken up in water, basified with saturated sodium hydrogen carbonate solution, and extracted with ethyl acetate. The combined ethyl acetate layers were washed with brine, dried over MgSO4, and concentrated under reduced pressure to afford 3-amino-2-fluorophenol (2.70 g, 100%) as a brown solid which was taken on without further purification. 1H NMR (400 MHz, DMSO-d6) δ 9.36 (brs, 1H), 6.62 (dd, J=8, 8 Hz, 1H), 6.12-6.23 (m, 2H), 5.14 (brs, 2H); LC-MS (ESI) m/z 128 (M+H)+.

후처리

  1. customThe reaction mixture was quenched via the addition of methanol
  2. concentrationAfter concentration under reduced pressure
  3. extractionextracted with ethyl acetate
  4. washThe combined ethyl acetate layers were washed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-c9b1ba753dc24eeeb81346a4b9e5f59e
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09320739B2

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