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Ammonia → 2-[(1,2-Dichloroethenyl)oxy]benzene-1-sulfonamide

HRID 325805
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HRID 325805 반응식
[Cl:1][C:2]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[S:12](Cl)(=[O:14])=[O:13])=[CH:3][Cl:4].O.[NH3:17]>C(Cl)Cl>[Cl:1][C:2]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[S:12]([NH2:17])(=[O:14])=[O:13])=[CH:3][Cl:4]
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참가 물질

5

반응물 3

HCID 222AmmoniaHCID 962WaterHCID 540123692-[(1,2-Dichloroethenyl)oxy]benzene-1-sulfonyl chloride

생성물 1

HCID 537128512-[(1,2-Dichloroethenyl)oxy]benzene-1-sulfonamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 17.5 g of 2-(1,2-dichlorovinyloxy)phenylsulfonyl-chloride in 150 ml of methylenechloride is added slowly to a mixture of 30 ml of methylene chloride, 50 ml of water and 50 ml of 30% aqueous ammonia. The reaction mixture is stirred for 6 hours at a temperature of 20°-25° C. The organic phase is washed with water, dried over sodium sulfate and evaporated to a volume of 40 ml. The crystallised 2-(1,2-dichlorovinyloxy)phenylsulfonamide is separated and dried. Yield: 12.5 g, m.p. 147°-149° C.

후처리

  1. washThe organic phase is washed with water
  2. dry with materialdried over sodium sulfate
  3. customevaporated to a volume of 40 ml
  4. customThe crystallised 2-(1,2-dichlorovinyloxy)phenylsulfonamide is separated
  5. customdried

출처 및 근거

ORD 기록
ord-9a4244b6d8bf42b5b6fc52a1cd35348c
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04443245

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