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Dimethylformamide → alpha-(2-Benzoyloxy-5-chlorosulfonylphenylazo)-beta-benzoyloxycinnamonitrile

HRID 2052197
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HRID 2052197 반응식
[C:1]([O:9][C:10]1[C:11]([N:19]=[N:20][C:21](=[C:24]([O:31][C:32](=[O:39])[C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:22]#[N:23])=[CH:12][C:13](=[S:16](=[O:18])=[O:17])[CH2:14][CH:15]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C)C=O.S(Cl)([Cl:47])=O>>[C:1]([O:9][C:10]1[CH:15]=[CH:14][C:13]([S:16]([Cl:47])(=[O:18])=[O:17])=[CH:12][C:11]=1[N:19]=[N:20][C:21](=[C:24]([O:31][C:32](=[O:39])[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[C:22]#[N:23])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 86736451alpha-(2-Benzoyloxy-5-sulfonylphenylazo)-beta-benzoyloxycinnamonitrile

생성물 1

HCID 54435792alpha-(2-Benzoyloxy-5-chlorosulfonylphenylazo)-beta-benzoyloxycinnamonitrile

실험 절차

To a solution of α-(2-benzoyloxy-5-sulfonylphenylazo)β-benzoyloxycinnamonitrile (10 g) in 50 ml of thionyl chloride was added 3 ml of dimethylformamide. The reaction mixture was allowed to stir at room temperature for 31/2 hours. The solvent was evaporated to dryness under vacuum at room temperature. The residue was diluted with ethyl ether (50 ml) to form a white precipitate. The product was filtered off and dried to yield 9.4 g, m.p. 153° to 155° C.

후처리

  1. customThe solvent was evaporated to dryness under vacuum at room temperature
  2. additionThe residue was diluted with ethyl ether (50 ml)
  3. customto form a white precipitate
  4. filtrationThe product was filtered off
  5. customdried
  6. customto yield 9.4 g, m.p. 153° to 155° C.

출처 및 근거

ORD 기록
ord-67ae8af2214545e29c52b1c8bafc50ed
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04183755

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