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2-Chloroacetophenone → HCID 20485523, 화합물

HRID 647133
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인쇄 미리보기

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HRID 647133 반응식
[CH2:1]([Cl:10])[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3].[O:11]1[CH2:16][CH2:15][N:14]([C:17]2[S:21][S:20][C:19](=[S:22])[CH:18]=2)[CH2:13][CH2:12]1>C(O)C>[Cl-:10].[CH2:1]([S:22][C:19]1[S:20][S:21][C:17](=[N+:14]2[CH2:15][CH2:16][O:11][CH2:12][CH2:13]2)[CH:18]=1)[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 107572-ChloroacetophenoneHCID 12863631HCID 12863631, 화합물

생성물 1

HCID 20485523HCID 20485523, 화합물수율 85.2%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
10 °C

실험 절차

Phenacyl chloride (10.5 g) is added to a suspension of 5-morpholino-1,2-dithiol-3-thione (9.85 g) in ethanol (200 cc), and the reaction mixture is kept under reflux for 3 hours. After cooling to a temperature of about 10° C., the insoluble product formed is filtered off and washed with ethanol (30 cc). After drying, N-(5-phenacylthio-1,2-dithiol-3-ylidene)-morpholinium chloride (14.3 g) is obtained, which melts at 138° C. and is solvated by 9% of ethanol.

후처리

  1. temperatureunder reflux for 3 hours
  2. customthe insoluble product formed
  3. filtrationis filtered off
  4. washwashed with ethanol (30 cc)
  5. customAfter drying

출처 및 근거

ORD 기록
ord-733ae00844864ca0a73c330aca556d41
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04407797

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