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Acetic Anhydride → 5-Chloro-2-(3-fluorophenyl)-4H-3,1-benzoxazin-4-one

HRID 1902389
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반응식

HRID 1902389 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:18]=[CH:19][CH:20]=1)[C:5]([NH:7][C:8]1[C:9](=[C:13]([Cl:17])[CH:14]=[CH:15][CH:16]=1)[C:10]([OH:12])=[O:11])=O.C(OC(=O)C)(=O)C>>[F:1][C:2]1[CH:3]=[C:4]([C:5]2[O:11][C:10](=[O:12])[C:9]3[C:13]([Cl:17])=[CH:14][CH:15]=[CH:16][C:8]=3[N:7]=2)[CH:18]=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 12837108HCID 12837108, 화합물

생성물 1

HCID 128371115-Chloro-2-(3-fluorophenyl)-4H-3,1-benzoxazin-4-one수율 86.7%

실험 절차

29 parts of N-(3'-fluorobenzoyl)-6-chloroanthranilic acid in 250 parts of acetic anhydride are stirred under reflux for 21/2 hours. The mixture is evaporated down under reduced pressure, the residue is taken up in methylene chloride and this solution is washed with twice 100 parts by volume of 0.5 N sodium hydroxide solution and then with water. Thereafter, the solution is chromatographed on neutral alumina, giving 23.6 parts of 2-(3'-fluorophenyl)-5-chloro-4H-3,1-benzoxazin-4-one, of melting point 123°-125° C.; yield: 86.7% of theory.

후처리

  1. temperatureunder reflux for 21/2 hours
  2. customThe mixture is evaporated down under reduced pressure
  3. wash
this solution is washed with twice 100 parts by volume of 0.5 N sodium hydroxide solution
  • customThereafter, the solution is chromatographed on neutral alumina
  • 출처 및 근거

    ORD 기록
    ord-2914e4ed66b545bab2de8741a8a7fc2e
    출처 데이터셋
    uspto-grants-1982_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04363651

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