Benzoyl Peroxide → 2-Bromomethyl-5-nitro-benzenesulfonic Acid, 2,2-Dimethylpropyl Ester

HRID 277583노트

반응식

HRID 277583 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O:14][CH2:15][C:16]([CH3:19])([CH3:18])[CH3:17])(=[O:13])=[O:12].C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[Br:38]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.C(OCC)(=O)C>[Br:38][CH2:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O:14][CH2:15][C:16]([CH3:19])([CH3:18])[CH3:17])(=[O:13])=[O:12]

참가 물질

6

실험 절차

To a solution of 2-methyl-5-nitro-benzenesulfonic acid, 2,2-dimethylpropyl ester, Example 24 (1.0 g, 3.48 mmol) in dry carbon tetrachloride (50 mL) was added 126 mg (0.52 mmol) of benzoyl peroxide and 712 mg (4.0 mmol) of recrystallized N-bromosuccinimide. A reflux condensor was attached and the mixture was heated to reflux and stirred overnight. After cooling to room temperature the reaction mixture was diluted with ethyl acetate (250 mL) and washed with water, followed by saturated sodium bicarbonate, and then brine. The organic layer was dried (MgSO4) and concentrated to dryness on a rotary evaporator. Purification by flash column chromatography using 10% ethyl acetate in hexanes gave 560 mg (44%) of the title compound as a white solid: 1HNMR (CDCl3): d 8.83 (d, J=2 Hz, 1H), 8.48 (dd, J=2 Hz, 9 Hz, 1H), 7.92 (d, J=9 Hz, 1H), 4.96 (s, 2H), 3.85 (s, 2H), 1.0 (s, 9H); MS (ES-NEG): [M−H] 364/366; Anal. Calc. for C12H16BrNO5S: C, 39.35; H, 4.40; N, 3.82. Found: C, 39.88; H, 4.16; N, 3.85.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux
  3. washwashed with water
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated to dryness on a rotary evaporator
  6. customPurification by flash column chromatography

출처 및 근거

ORD 기록
ord-6b688e3473e84eedbf8508862a80a047
출처 데이터셋
uspto-grants-2002_03
특허 번호
US06355633B1

반응 노트

불러오는 중…