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Methyl p-toluenesulfonate → 1,1-Dimethyl-1,2,3,4-tetrahydro-2-hydroxymethylquinolinium p-toluenesulfonate

HRID 2081501
노트
인쇄 미리보기

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HRID 2081501 반응식
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][CH:3]1[CH2:12][OH:13].[C:14]1([CH3:25])[CH:19]=[CH:18][C:17]([S:20]([O:23]C)(=[O:22])=[O:21])=[CH:16][CH:15]=1>>[C:14]1([CH3:25])[CH:15]=[CH:16][C:17]([S:20]([O-:23])(=[O:21])=[O:22])=[CH:18][CH:19]=1.[CH3:1][N+:2]1([CH3:14])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][CH:3]1[CH2:12][OH:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6645Methyl p-toluenesulfonateHCID 124157581-Methyl-1,2,3,4-tetrahydro-2-quinolinemethanol

생성물 1

HCID 150522411,1-Dimethyl-1,2,3,4-tetrahydro-2-hydroxymethylquinolinium p-toluenesulfonate수율 202%

반응 조건

온도
100 °C

실험 절차

A mixture of 1.3 g of 1-methyl-1,2,3,4-tetrahydro-2-quinolinemethanol and 1.37 g of methyl p-toluenesulfonate was heated at 100° C. for 6 hours. The solvent was removed from the reaction mixture by decantation, and the residue was washed with ether to give 2.7 g of the desired compound as a dark red oil.

후처리

custom
The solvent was removed from the reaction mixture by decantation
  • washthe residue was washed with ether
  • 출처 및 근거

    ORD 기록
    ord-57aab7aa79b9419383473f8bf96381bd
    출처 데이터셋
    uspto-grants-1993_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05183811

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