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Thionyl Chloride → p-(1-Chloroethyl)phenyl 2-thienyl ketone

HRID 258925
노트
인쇄 미리보기

반응식

HRID 258925 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:8]1[CH:13]=[CH:12][C:11]([CH:14](O)[CH3:15])=[CH:10][CH:9]=1)=[O:7].S(Cl)([Cl:19])=O>C1C=CC=CC=1>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:8]1[CH:13]=[CH:12][C:11]([CH:14]([Cl:19])[CH3:15])=[CH:10][CH:9]=1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 12232927p-(1-Hydroxyethyl)phenyl 2-thienyl ketone

생성물 1

HCID 12232928p-(1-Chloroethyl)phenyl 2-thienyl ketone

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To a stirred and cooled solution of 43.7 parts of p-(1-hydroxyethyl)phenyl 2-thienyl ketone in 180 parts of dry benzene are added dropwise 16 parts of thionyl chloride. Upon completion, stirring is continued overnight at room temperature. The reaction mixture is evaporated. The residue is taken up in toluene and the latter is evaporated once more. The latter residue is distilled and the distillate is crystallized from ethanol at room temperature, yielding p-(1-chloroethyl)phenyl 2-thienyl ketone; mp. 60° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. stirringUpon completion, stirring
  2. customThe reaction mixture is evaporated
  3. customthe latter is evaporated once more
  4. distillationThe latter residue is distilled
  5. customthe distillate is crystallized from ethanol at room temperature

출처 및 근거

ORD 기록
ord-63d771a49ed6413dbdab59ce19047816
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04035376

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