홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

p-Toluenesulfonic acid monohydrate → 4-Fluorophenyldiphenylsulfonium 4-toluene-sulfonate

HRID 1920615
노트
인쇄 미리보기

반응식

HRID 1920615 반응식
[Cl-].[F:2][C:3]1[CH:8]=[CH:7][C:6]([S+:9]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:5][CH:4]=1.O.[C:23]1([CH3:33])[CH:28]=[CH:27][C:26]([S:29]([OH:32])(=[O:31])=[O:30])=[CH:25][CH:24]=1>>[C:23]1([CH3:33])[CH:24]=[CH:25][C:26]([S:29]([O-:32])(=[O:30])=[O:31])=[CH:27][CH:28]=1.[F:2][C:3]1[CH:8]=[CH:7][C:6]([S+:9]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 866496604-Fluorophenyldiphenylsulfonium chloride

생성물 1

HCID 187593244-Fluorophenyldiphenylsulfonium 4-toluene-sulfonate

실험 절차

The 4-fluorophenyldiphenylsulfonium chloride aqueous solution in Synthesis Example 1 was combined with 4-toluenesulfonic acid monohydrate, followed by extraction with dichloromethane. The organic layer was washed with water, after which the solvent was distilled off in vacuum. Isopropyl ether was added to the residue for crystallization. Filtration and drying yielded the target compound.

후처리

  1. extractionfollowed by extraction with dichloromethane
  2. washThe organic layer was washed with water
  3. distillationafter which the solvent was distilled off in vacuum
addition
Isopropyl ether was added to the residue for crystallization
  • filtrationFiltration
  • customdrying
  • customyielded the target compound
  • 출처 및 근거

    ORD 기록
    ord-e4d0aa0b8d964600aea8289334b6cc85
    출처 데이터셋
    uspto-grants-2012_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08173354B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트