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Sulfuric Acid → HCID 86739048, 화합물

HRID 647134
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HRID 647134 반응식
[S:1](=[O:5])(=[O:4])([OH:3])[OH:2].[Cl-].[CH2:7]([S:16][C:17]1[S:21][S:20][C:19](=[N+:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)[CH:18]=1)[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9]>C(O)C>[S:1]([O-:5])([OH:4])(=[O:3])=[O:2].[CH2:7]([S:16][C:17]1[S:21][S:20][C:19](=[N+:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)[CH:18]=1)[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 20485523HCID 20485523, 화합물

생성물 1

HCID 86739048HCID 86739048, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
10 °C

실험 절차

A solution of concentrated sulphuric acid (d=1.83; 0.2 cc) in ethanol (5 cc) is added to a solution of N-(5-phenacylthio-1,2-dithiol-3-ylidene)-morpholinium chloride (0.75 g) in ethanol (20 cc) under reflux. After cooling to a temperature of about 10° C., the insoluble product formed is filtered off and washed with ethanol (4 cc). After drying, N-(5-phenacylthio-1,2-dithiol-3-ylidene)-morpholinium hydrogensulphate (0.8 g), melting at 192° C., is obtained.

후처리

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

출처 및 근거

ORD 기록
ord-d26f3e6767314094b402c5415b32ce25
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04407797

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