m-Chloroperbenzoic acid → 3-Chlorobenzoic Acid

HRID 389357노트

반응식

HRID 389357 반응식
[C:1]([O:6][CH:7]([O:9][C:10]([O:12][CH:13]1[CH2:18][C:17](=[O:19])[NH:16][C:14]1=[O:15])=[O:11])[CH3:8])(=[O:5])[CH:2]([CH3:4])[CH3:3].ON1C(=O)CCC1=O.C(=O)(SC(C)(C)C)OC(OC(=O)C(C)C)C.[Cl:44][C:45]1[CH:50]=[CH:49][CH:48]=[C:47]([C:51]([O:53]O)=[O:52])[CH:46]=1>C(Cl)Cl.CCOCC>[C:1]([O:6][CH:7]([O:9][C:10]([O:12][CH:13]1[CH2:18][C:17](=[O:19])[NH:16][C:14]1=[O:15])=[O:11])[CH3:8])(=[O:5])[CH:2]([CH3:4])[CH3:3].[Cl:44][C:45]1[CH:46]=[C:47]([CH:48]=[CH:49][CH:50]=1)[C:51]([OH:53])=[O:52]

참가 물질

8

실험 절차

In still another alternative synthesis of (10), N-hydroxysuccinimide (230 mg, 2 mmol) was added to a solution of compound (8) (248 mg, 1 mmol) in CH2Cl2 (10 mL) was added and the reaction mixture cooled to 0° C. m-Chloroperbenzoic acid (670 mg, 3 mmol, commercial grade: 77% in water) was added over a period of 10 min and the mixture allowed to stir at room temperature for 16 h. The reaction mixture was diluted with ether (50 mL) and washed with water (2×10 mL), saturated sodium bicarbonate solution (10 mL) and brine (10 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give the title compound (10) together with m-chlorobenzoic acid. The crude product mixture was purified by column chromatography on silica gel, eluting with 4:6 EtOAc:hexane. Residual m-chlorobenzoic acid was removed by repeated crystallizations from a mixture of tert-butyl methyl ether and hexane which resulted in analytically pure product (30 mg, 11%).

후처리

  1. additionwas added
  2. additionwas added over a period of 10 min
  3. washwashed with water (2×10 mL), saturated sodium bicarbonate solution (10 mL) and brine (10 mL)
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e3e2fb32e1734e58aba26afd5e62ae0f
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08378137B2

반응 노트

불러오는 중…