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Acetic Anhydride → Flufenisal

HRID 442275
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HRID 442275 반응식
[OH:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:18](OC(=O)C)(=[O:20])[CH3:19]>N1C=CC=CC=1>[C:18]([O:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)=[CH:7][C:3]=1[C:4]([OH:6])=[O:5])(=[O:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 27826944'-Fluoro-4-hydroxy-[1,1'-biphenyl]-3-carboxylic acid

생성물 1

HCID 31185Flufenisal

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 3.0 grams of 2-hydroxy-5-(4'-fluorophenyl)-benzoic acid in 12 ml. of pyridine and 8 ml. of acetic anhydride is heated on a steam bath for 20 minutes. The mixture is then poured onto ice and the product extracted with methylene chloride. The methylene chloride solution is dried and then evaporated. The residue is recrystallized from benzene to yield 2-acetoxy 5-(4'-fluorophenyl)-benzoic acid (m.p. 134° - 137° C.).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
addition
The mixture is then poured onto ice
  • extractionthe product extracted with methylene chloride
  • dry with materialThe methylene chloride solution is dried
  • customevaporated
  • customThe residue is recrystallized from benzene
  • 출처 및 근거

    ORD 기록
    ord-7ba937c926934c758493afec3417b601
    출처 데이터셋
    uspto-grants-1977_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04044049

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