Boron tribromide → 3-Amino-2-fluorophenol

HRID 871636노트

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HRID 871636 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-7edb00f799bf496798c41dbe2413b14b
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08969587B2

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