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Styrene-4-sulfonyl chloride → N-hydroxy-2-phenylsuccinimide p-styrenesulfonate

HRID 359669
노트
인쇄 미리보기

반응식

HRID 359669 반응식
[OH:1][N:2]1[C:6](=[O:7])[CH2:5][CH:4]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:3]1=[O:14].[CH2:15]=[CH:16][C:17]1[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1>CC(C)=O>[OH:1][N:2]1[C:6](=[O:7])[CH2:5][CH:4]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:3]1=[O:14].[CH2:15]=[CH:16][C:17]1[CH:22]=[CH:21][C:20]([S:23]([O-:25])(=[O:1])=[O:24])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9855777Styrene-4-sulfonyl chlorideHCID 12391645N-hydroxy-2-phenylsuccinimide

생성물 1

HCID 86744681N-hydroxy-2-phenylsuccinimide p-styrenesulfonate수율 115.6%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

50 ml of acetone was added to 3.8 g of N-hydroxy-2-phenylsuccinimide and 4.1 g of p-styrenesulfonyl chloride and then the same procedure as that of Preparation Example 1 was repeated to obtain 4.3 g of N-hydroxy-2-phenylsuccinimide-p-styrenesulfonate.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customthe same procedure as that of Preparation Example 1
  • 출처 및 근거

    ORD 기록
    ord-4f2cd66673a246afa7467404582ff84c
    출처 데이터셋
    uspto-grants-1991_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05002853

    반응 노트

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