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Thionyl Chloride → HCID 70637434, 화합물

HRID 461738
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HRID 461738 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:8]1[C:9]([CH3:17])=[CH:10][CH:11]=[CH:12][C:13]=1[CH:14](O)[CH3:15])=[O:7].S(Cl)([Cl:20])=O>C1C=CC=CC=1>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:8]1[C:9]([CH3:17])=[CH:10][CH:11]=[CH:12][C:13]=1[CH:14]([Cl:20])[CH3:15])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 70637620HCID 70637620, 화합물

생성물 1

HCID 70637434HCID 70637434, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 14.7 parts of 3-(1-hydroxyethyl)-o-tolyl 2-thienyl ketone and 126 parts of benzene is stirred while cooling on an ice-bath. Then 9.5 parts of thionyl chloride are added and the whole is stirred further over week-end at room temperature. The reaction mixture is evaporated in vacuo, yielding 3-(1-chloroethyl)-o-tolyl 2-thienyl ketone as a residue.

후처리

  1. temperaturewhile cooling on an ice-bath
  2. stirringthe whole is stirred further over week-end at room temperature
  3. customThe reaction mixture is evaporated in vacuo

출처 및 근거

ORD 기록
ord-a41ef484ee9a49528a416df6799ae2ec
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04064132

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