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2-Bromopropanoyl chloride → N-(2,3-dihydro-2,2-dimethylbenzofuran-7-yl)sulfonyl-2-bromopropionamide

HRID 1252342
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반응식

HRID 1252342 반응식
[NH2:1][S:2]([C:5]1[C:13]2[O:12][C:11]([CH3:15])([CH3:14])[CH2:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)(=[O:4])=[O:3].[Br:16][CH:17]([CH3:21])[C:18](Cl)=[O:19]>>[CH3:14][C:11]1([CH3:15])[CH2:10][C:9]2[CH:8]=[CH:7][CH:6]=[C:5]([S:2]([NH:1][C:18](=[O:19])[CH:17]([Br:16])[CH3:21])(=[O:4])=[O:3])[C:13]=2[O:12]1
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참가 물질

3

반응물 2

HCID 979802-Bromopropanoyl chlorideHCID 134241802,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamide

생성물 1

HCID 15611040N-(2,3-dihydro-2,2-dimethylbenzofuran-7-yl)sulfonyl-2-bromopropionamide

실험 절차

A stirred slurry of 0.39 gram (0.0017 mole) of 7-aminosulfonyl-2,3-dihydro-2,2-dimethylbenzofuran and 1 ml of 2-bromopropionyl chloride was heated at 96° for 35 minutes, then at reflux for 30 minutes. The reaction mixture was cooled to ambient temperature and washed repeatedly with petroleum ether to remove excess acid chloride. The residue was 0.53 gram of N-(2,3-dihydro-2,2-dimethylbenzofuran-7-yl)sulfonyl-2-bromopropionamide; m.p. 224°-226° C.

후처리

  1. temperatureat reflux for 30 minutes
  2. washwashed repeatedly with petroleum ether
  3. customto remove excess acid chloride

출처 및 근거

ORD 기록
ord-927946299c6e47149999ba99b1b9c449
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04743291

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