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4-Methylphenyl isocyanate → N'-t-butyl-N'-benzoyl-N-[N-(4-tolyl)aminocarbonyl]hydrazine

HRID 21664
Notes
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Reaction equation

HRID 21664 reaction equation
[C:1]([N:5]([C:7](=[O:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[NH2:6])([CH3:4])([CH3:3])[CH3:2].[CH3:15][C:16]1[CH:21]=[CH:20][C:19]([N:22]=[C:23]=[O:24])=[CH:18][CH:17]=1>C(OCC)C>[C:1]([N:5]([C:7](=[O:14])[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[NH:6][C:23]([NH:22][C:19]1[CH:20]=[CH:21][C:16]([CH3:15])=[CH:17][CH:18]=1)=[O:24])([CH3:4])([CH3:2])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 693254-Methylphenyl isocyanateHCID 1275961N-(tert-butyl)benzohydrazide

Product 1

HCID 15452014N'-t-butyl-N'-benzoyl-N-[N-(4-tolyl)aminocarbonyl]hydrazineYield 36.9%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

N't-butyl-N'-benzoylhydrazine (0.8 g) and p-methylphenylisocyanate (0.9 g) were stirred in diethylether (10 ml) at 23° C. for 15 hours. The reaction mixture was diluted with ether and filtered to afford 0.5 g of solid product: m.p. 208°-210° C.

Workup

  1. filtrationfiltered

Sources & evidence

ORD record
ord-aedc6c47ee764eac9fb8f6848422fcff
Source dataset
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05424333

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes