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Acetic Anhydride → HCID 15700644, 화합물

HRID 236788
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반응식

HRID 236788 반응식
C(O[C:5](=[O:7])[CH3:6])(=O)C.[N:8]1([C:14]2[C:15]3[CH:28]=[CH:27][CH:26]=[CH:25][C:16]=3[S:17][C:18]=2[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1>C(Cl)Cl>[C:5]([N:11]1[CH2:12][CH2:13][N:8]([C:14]2[C:15]3[CH:28]=[CH:27][CH:26]=[CH:25][C:16]=3[S:17][C:18]=2[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:9][CH2:10]1)(=[O:7])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 157006411-(2-Phenyl-1-benzothiophen-3-yl)piperazine

생성물 1

HCID 15700644HCID 15700644, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6.15 g (60 mmole) of acetic anhydride are mixed with a solution of 11.8 g (40 mmole) of 3-piperazino-2-phenyl-benzo(b)thiophene in 50 milliliters of methylene chloride and left for 2 hours at ambient temperature. After washing with dilute ammonia the organic phase is dried over Na2SO4 and evaporated: 13.2 g (98% of theory) of colourless needles, mp 167°-169° (CCl4).

후처리

wash
After washing with dilute ammonia the organic phase
  • dry with materialis dried over Na2SO4
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-0e22c63216724c42a8e54d4fe14e7029
    출처 데이터셋
    uspto-grants-1979_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04157399

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