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Hydrazine hydrate (1:1) → 4,4'-Dimethylbenzil hydrazone

HRID 436380
Notes
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Reaction equation

HRID 436380 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)=[O:11])=O)=[CH:4][CH:3]=1.O.[NH2:20][NH2:21]>C(O)C>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[N:20][NH2:21])[C:10]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)=[O:11])=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24654Hydrazine hydrate (1:1)HCID 769961,2-Bis(4-methylphenyl)-1,2-ethanedione

Product 1

HCID 41636394,4'-Dimethylbenzil hydrazone

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
0 °C

Procedure

To a hot solution of 10 g 4,4'-dimethylbenzil in 20 ml of ethanol is added 2.1 g of hydrazine hydrate. After a few minutes at reflux, a solid begins to crystallize. Heating is continued for 10 min. and the solution cooled slowly to 0° C. The solid is filtered off and washed with cold ethanol. The product is recrystallized from ethanol. Yield 7.1 g. M.P. 137°-140°.

Workup

  1. temperatureAfter a few minutes at reflux
  2. customto crystallize
  3. temperatureHeating
  4. filtrationThe solid is filtered off
  5. washwashed with cold ethanol
  6. customThe product is recrystallized from ethanol

Sources & evidence

ORD record
ord-dcbad63dca914678bef8fcb4b5e23730
Source dataset
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04009022

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes