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Tributylphosphine → Tributyl((4-chlorophenylthio)methyl)phosphonium chloride

HRID 46407
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인쇄 미리보기

반응식

HRID 46407 반응식
[CH2:1]([P:5]([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].[Cl:14][C:15]1[CH:20]=[CH:19][C:18]([S:21][CH2:22]Cl)=[CH:17][CH:16]=1>O1CCOCC1.CCCCCC>[Cl-:14].[CH2:10]([P+:5]([CH2:1][CH2:2][CH2:3][CH3:4])([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:22][S:21][C:18]1[CH:19]=[CH:20][C:15]([Cl:14])=[CH:16][CH:17]=1)[CH2:11][CH2:12][CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 13831TributylphosphineHCID 23610Benzene, 1-chloro-4-((chloromethyl)thio)-

생성물 1

HCID 20386972Tributyl((4-chlorophenylthio)methyl)phosphonium chloride

시약·촉매·용매 2

HCID 8058Hexane용매HCID 312751,4-Dioxane용매

실험 절차

A solution of 8.45 g of tri(n-butyl)phosphine and 8.33 g of chloromethyl 4-chlorophenyl sulfide in 25 ml of p-dioxane was stirred and refluxed (101°-102° C.) for 20 hours. The mixture was cooled to room temperature and diluted with 100 ml of hexane. The white precipitate was filtered and dried to give 1, as a solid, mp 113°-114° C.

후처리

  1. temperaturerefluxed (101°-102° C.) for 20 hours
  2. filtrationThe white precipitate was filtered
  3. customdried
  4. customto give 1

출처 및 근거

ORD 기록
ord-c3b2990a92984880a10a534b9361c913
출처 데이터셋
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04173463

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