Methylamine → 3-bromo-N-methylbenzene-1-sulfonamide

HRID 78320노트

반응식

HRID 78320 반응식
[Br:1][C:2]1[CH:3]=[C:4]([S:8](Cl)(=[O:10])=[O:9])[CH:5]=[CH:6][CH:7]=1.[CH3:12][NH2:13]>C1COCC1>[CH3:12][NH:13][S:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=1)(=[O:10])=[O:9]

참가 물질

4

실험 절차

To a solution of 3-bromobenzenesulfonyl chloride (2.5 g, 11.2 mmol) in THF (15 mL) at 0° C. was added methylamine (2.0 M in THF; 28 mL, 56 mmol). The resulting solution was allowed to warm to room temp. and was stirred at room temp. overnight. The resulting mixture was separated between EtOAc (25 mL) and a 1 M HCl solution (25 mL). The aqueous phase was back-extracted with EtOAc (2×25 mL). The combined organic phases were sequentially washed with water (2×25 mL) and a saturated NaCl solution (25 mL), dried (MgSO4) and concentrated under reduced pressure to give N-methyl-3-bromobenzenesulfonamide as a white solid (2.8 g, 99%).

후처리

  1. temperatureto warm to room temp.
  2. customThe resulting mixture was separated between EtOAc (25 mL)
  3. extractionThe aqueous phase was back-extracted with EtOAc (2×25 mL)
  4. washThe combined organic phases were sequentially washed with water (2×25 mL)
  5. dry with materiala saturated NaCl solution (25 mL), dried (MgSO4)
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-1c8365b710764efca9fb600eaa2c80d1
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841330B2

반응 노트

불러오는 중…