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Methylhydrazine → (Aminomethylamino)((4-chlorophenyl)amino)methane-1-thione

HRID 1981335
Notes
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Reaction equation

HRID 1981335 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]=[C:9]=[S:10])=[CH:4][CH:3]=1.[CH3:11][NH:12][NH2:13]>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([N:12]([CH3:11])[NH2:13])=[S:10])=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6061MethylhydrazineHCID 164804-Chlorophenyl isothiocyanate

Product 1

HCID 2060916(Aminomethylamino)((4-chlorophenyl)amino)methane-1-thione

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 4-chlorophenylisothiocyanate (17.0 g, 0.10 mole) and methylhydrazine (5.0 g, 0.11 mole) in 80 ml of ethanol was stirred at room temperature for two hours. The reaction mixture was filtered to collect colorless crystalline N-(4-chlorophenyl)-1-methylhydrazinecarbothioamide (18.4 g, mp 152°-154° C.).

Workup

  1. filtrationThe reaction mixture was filtered
  2. customto collect colorless crystalline N-(4-chlorophenyl)-1-methylhydrazinecarbothioamide (18.4 g, mp 152°-154° C.)

Sources & evidence

ORD record
ord-6d4d2704efcb46fc958055c8e078625f
Source dataset
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04514419

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes