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Cinnamoylbenzene → HCID 3798265, compound

HRID 2295473
Notes
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Reaction equation

HRID 2295473 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7189CinnamoylbenzeneHCID 7516Phenylhydrazine

Product 1

HCID 3798265HCID 3798265, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

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.

Workup

  1. customover 5 hours
  2. temperature
to cool
  • customreaction product
  • filtrationThe sediment was filtered
  • washwashed with ethanol
  • customdried
  • Sources & evidence

    ORD record
    ord-d52816a7584c405f995ea4670740be4f
    Source dataset
    uspto-grants-1984_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04425179

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes