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Methanol → HCID 21456046, 화합물

HRID 435716
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HRID 435716 반응식
[C:1]1([S:7][C:8]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:19])[F:18])=[CH:13][C:9]=2[C:10]([OH:12])=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[CH3:26]O>>[C:1]1([S:7][C:8]2[CH:16]=[CH:15][C:14]([C:17]([F:20])([F:18])[F:19])=[CH:13][C:9]=2[C:10]([O:12][CH3:26])=[O:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 1042312-Phenylthio-5-trifluoromethylbenzoic acid

생성물 1

HCID 21456046HCID 21456046, 화합물

실험 절차

100 g of 2-(phenylthio)-5-trifluoromethyl-benzoic acid, 750 ml of absolute methanol and 100 ml of sulphuric acid are heated under reflux for 24 hours. The solution is concentrated under reduced pressure and treated with water and benzene. After equilibration, the organic phase is washed successively with saturated aqueous sodium chloride solution, saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution. The benzene phase is subsequently dried over sodium sulphate, filtered and evaporated. There is obtained methyl 2-(phenylthio)-5-trifluoromethyl-benzoate as a yellow oil.

후처리

  • temperatureunder reflux for 24 hours
  • concentrationThe solution is concentrated under reduced pressure
  • additiontreated with water and benzene
  • washAfter equilibration, the organic phase is washed successively with saturated aqueous sodium chloride solution, saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution
  • dry with materialThe benzene phase is subsequently dried over sodium sulphate
  • filtrationfiltered
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-963e44ae621d424e9b743bbb3bce6000
    출처 데이터셋
    uspto-grants-1977_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04006144

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