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Thionyl Chloride → 5-chloro-3-methylthio-5H-dibenzo[a,d]cycloheptene

HRID 2290288
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인쇄 미리보기

반응식

HRID 2290288 반응식
S(Cl)([Cl:3])=O.[CH3:5][S:6][C:7]1[CH:8]=[CH:9][C:10]2[CH:16]=[CH:15][C:14]3[CH:17]=[CH:18][CH:19]=[CH:20][C:13]=3[CH:12](O)[C:11]=2[CH:22]=1>C1C=CC=CC=1>[Cl:3][CH:12]1[C:11]2[CH:22]=[C:7]([S:6][CH3:5])[CH:8]=[CH:9][C:10]=2[CH:16]=[CH:15][C:14]2[CH:17]=[CH:18][CH:19]=[CH:20][C:13]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 202322443-methylthio-5H-dibenzo[a,d]cyclohepten-5-ol

생성물 1

HCID 202322695-chloro-3-methylthio-5H-dibenzo[a,d]cycloheptene

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

Molar excess (5 milliliters) of thionyl chloride was added to a solution of the 3-methylthio-5H-dibenzo[a,d]cyclohepten-5-ol intermediate in 45 milliliters of benzene and the resulting mixture heated under reflux for two hours to obtain a 5-chloro-3-methylthio-5H-dibenzo[a,d]cycloheptene (chloro compound) intermediate in the reaction mixture. The reaction mixture was subjected to reduced pressure to co-evaporate benzene and unreacted thionyl chloride, and the procedure repeated with several additions of benzene to obtain a purified chloro compound intermediate.

후처리

  1. temperaturethe resulting mixture heated
  2. temperatureunder reflux for two hours

출처 및 근거

ORD 기록
ord-72d4825da18f4bbb83c4bd7b1fc15662
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616023

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