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Dimethyl(beta-oxophenethyl)sulphonium bromide → HCID 19047920, 화합물

HRID 1440887
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인쇄 미리보기

반응식

HRID 1440887 반응식
[CH2:1]([B-:5]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[Li+].[Br-].[CH3:26][S+:27]([CH3:37])[CH2:28][C:29]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:30]>O>[CH3:26][S+:27]([CH3:37])[CH2:28][C:29]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:30].[CH2:1]([B-:5]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 213007Dimethyl(beta-oxophenethyl)sulphonium bromideHCID 23668465HCID 23668465, 화합물

생성물 1

HCID 19047920HCID 19047920, 화합물수율 61.1%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

An aqueous solution of 5.424 g of lithium butyltriphenylborate in 100 ml of water was added to an aqueous solution of 5.090 g of dimethylphenacylsulfonium bromide in 200 ml of water, and the resultant mixture was stirred at room temperature for 30 minutes. The reaction mixture was filtered, and the resultant crystal was washed with water and dried to give 5.202 g of dimethylphenacylsulfonium-butyltriphenylborate as a white crystal.

후처리

  1. filtrationThe reaction mixture was filtered
  2. washthe resultant crystal was washed with water
  3. customdried

출처 및 근거

ORD 기록
ord-2bc82f63e82b478984cf9c2e224b354d
출처 데이터셋
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05500453

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