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m-Chloroperbenzoic acid → 2-Oxiranylmethoxyphenylsulfonamide

HRID 649292
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반응식

HRID 649292 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH2:12]([O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[S:22]([NH2:25])(=[O:24])=[O:23])[CH:13]=[CH2:14]>C(Cl)Cl>[O:9]1[CH2:14][CH:13]1[CH2:12][O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[S:22]([NH2:25])(=[O:23])=[O:24]
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 133217572-[(Prop-2-en-1-yl)oxy]benzene-1-sulfonamide

생성물 1

HCID 200403992-Oxiranylmethoxyphenylsulfonamide수율 78%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of 15.3 g of 3-chloroperbenzoic acid in 270 ml of absolute methylene chloride are added 14.2 g of 2-allyloxyphenylsulfonamide over 2 minutes. The solution is then heated to reflux for 3 hours, cooled, and then washed three times with saturated sodium carbonate solution and once with water. The organic phase is dried and concentrated, affording 11.9 g of 2-oxiranylmethoxyphenylsulfonamide with a melting point of 132°-133° C.

후처리

  1. temperatureThe solution is then heated
  2. temperatureto reflux for 3 hours
  3. temperaturecooled
  4. washwashed three times with saturated sodium carbonate solution
  5. customThe organic phase is dried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2b3febd65829459aa2bbb433a94be3fa
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04739068

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