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Thionyl Chloride → HCID 15619001, 화합물

HRID 435718
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HRID 435718 반응식
[C:1]1([S:7][C:8]2[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][C:9]=2[CH2:10]O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:22])=O>C1C=CC=CC=1>[C:1]1([S:7][C:8]2[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][C:9]=2[CH2:10][Cl:22])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 122239522-(Phenylthio)-5-(trifluoromethyl)benzenemethanol

생성물 1

HCID 15619001HCID 15619001, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

96 g of 2-(phenylthio)-5-trifluoromethyl-benzyl alcohol are dissolved in 450 ml of absolute benzene and heated to reflux. The solution thus obtained is treated dropwise over a period of 20 minutes with 48 ml of thionyl chloride and the mixture is subsequently stirred at reflux for 30 minutes. After cooling, the mixture is evaporated under reduced pressure. There is obtained 2-(phenylthio)-5-trifluoromethyl-benzyl chloride as a brown-yellow oil.

후처리

  1. temperatureheated to reflux
  2. customThe solution thus obtained
  3. temperatureat reflux for 30 minutes
  4. temperatureAfter cooling
  5. customthe mixture is evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3b912a9eb34546278b7e28fe7a7b6651
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04006144

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