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Acetic Anhydride → N-(2-chloro-4-fluorophenyl)-N-[(chloromethyl)sulfonyl]acetamide

HRID 1934843
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HRID 1934843 반응식
[Cl:1][CH2:2][S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][C:8]=1[Cl:14])(=[O:5])=[O:4].[C:15](OC(=O)C)(=[O:17])[CH3:16]>>[Cl:14][C:8]1[CH:9]=[C:10]([F:13])[CH:11]=[CH:12][C:7]=1[N:6]([S:3]([CH2:2][Cl:1])(=[O:4])=[O:5])[C:15](=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 187608471-chloro-N-(2-chloro-4-fluorophenyl)methanesulfonamide

생성물 1

HCID 18760837N-(2-chloro-4-fluorophenyl)-N-[(chloromethyl)sulfonyl]acetamide수율 80%

실험 절차

77.5 g (0.3 mol) of 1-chloro-N-(2-chloro-4-fluorophenyl)methanesulfonamide were dissolved in 204.2 g (2 mol) of acetic anhydride and refluxed for 4 hours. The excess acetic anhydride was distilled off under reduced pressure at 100° C. To the still hot residue was added ethanol with stirring and the product precipitated (seeding may aid in crystallization). The crude product was filtered off and washed with cold ethanol and dried to yield 72 g (80%) of the title compound as a solid melting at 89-92° C.

후처리

  1. temperaturerefluxed for 4 hours
  2. distillationThe excess acetic anhydride was distilled off under reduced pressure at 100° C
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • additionTo the still hot residue was added ethanol
  • customthe product precipitated
  • custom(seeding may aid in crystallization)
  • filtrationThe crude product was filtered off
  • washwashed with cold ethanol
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-d42488dd99bb4d0eb88c783b820796c5
    출처 데이터셋
    uspto-grants-2002_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06384234B1

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