Propanenitrile, 3-[(3-methylphenyl)amino]- → N-(2-cyanoethyl)-3-methylcarbanilic acid-[3-(trichloromethylcarbonylamino)-phenyl]-ester

HRID 2295697Notes

Reaction equation

HRID 2295697 reaction equation
[C:1]([CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[CH:7]=1)#[N:2].[Cl:13][C:14]([Cl:29])([Cl:28])[C:15]([NH:17][C:18]1[CH:19]=[C:20]([O:24][C:25](Cl)=[O:26])[CH:21]=[CH:22][CH:23]=1)=[O:16]>C(#N)C>[Cl:13][C:14]([Cl:28])([Cl:29])[C:15]([NH:17][C:18]1[CH:19]=[C:20]([O:24][C:25](=[O:26])[N:5]([CH2:4][CH2:3][C:1]#[N:2])[C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[CH:7]=2)[CH:21]=[CH:22][CH:23]=1)=[O:16]

Participants

4

Reactant 2

HCID 119683Propanenitrile, 3-[(3-methylphenyl)amino]-HCID 53923320HCID 53923320, compound

Product 1

HCID 20455825N-(2-cyanoethyl)-3-methylcarbanilic acid-[3-(trichloromethylcarbonylamino)-phenyl]-ester

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent2×

Procedure

Into a solution of 16.0 g N-(2-cyanoethyl)-3-methylaniline in 100 ml acetonitrile, 31.7 g chloroformic acid-3-(trichloromethylcarbonylamino)-phenyl ester taken up in 100 ml acetonitrile is added dropwise. The reaction mixture is heated to boiling for another 10 minutes, cooled, stirred in 500 ml ice water, the precipitate filtered and recrystallized from isopropanol.

Workup

  1. additionis added dropwise
  2. temperatureThe reaction mixture is heated
  3. temperaturecooled
  4. filtrationthe precipitate filtered
  5. customrecrystallized from isopropanol

Sources & evidence

ORD record
ord-87a68a68534f4ebf8a09bb014bc3920e
Source dataset
uspto-grants-1984_01
Patent number
US04426222

Reaction notes

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