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Cinnamoylbenzene → HCID 3798265, 화합물

HRID 2295473
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HRID 2295473 반응식
[CH:1](=[CH:8][C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:17]1([NH:23][NH2:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C(O)C>[C:17]1([N:23]2[CH:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH:8]=[C:1]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[NH:24]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7189CinnamoylbenzeneHCID 7516Phenylhydrazine

생성물 1

HCID 3798265HCID 3798265, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

20.8 g benzylideneacetophenone was condensed with 10.8 g phenylhydrazine in 400 ml boiling ethanol over 5 hours, and then allowed to cool. During the cooling process the desired reaction product separates. The sediment was filtered, washed with ethanol and dried.

후처리

  1. customover 5 hours
  2. temperatureto cool
  3. customreaction product
  4. filtrationThe sediment was filtered
  5. washwashed with ethanol
  6. customdried

출처 및 근거

ORD 기록
ord-d52816a7584c405f995ea4670740be4f
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04425179

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