Water → 4-Nitroaniline

HRID 866744Notes

Reaction equation

HRID 866744 reaction equation
[OH2:1].[C:2](#[N:5])[CH:3]=[CH2:4]>CC(C)=O>[CH:4]1[C:2]([NH2:5])=[CH:3][CH:4]=[C:2]([N+:5]([O-:1])=[O:1])[CH:3]=1

Participants

4

Procedure

A mixture of 120 parts of acrylonitrile and 1000 parts of acetone is introduced into the solution of the diazo derivative obtained from 276 parts of p-nitraniline. Then 40 parts of cupric chloride cyrstallised with 2 molecules of water are added and the mixture is kept vigorously stirred. The evolution of nitrogen is exothermal and the temperature must be maintained at 30°-32° C. by means of a cooling bath. After the diazonium chloride has disappeared (six hours), the yellow flakes which melt at 108° C. are filtered off. After recrystallising from methanol, 330 parts of 2-chloro-4'-nitro-3-phenyl-propionitrile are obtained which melts at 112° C. The product obtained is then dehydrohalogenated by means of 200 parts of crystalline sodium acetate in a mixture of 340 parts of water and 800 parts of ethyl alcohol. The mixture is heated under reflux for 12 hours and 225 parts of 4-nitro-cinnamonitrile which melts at 202° C. are isolated in the cold.

Sources & evidence

ORD record
ord-48eaaf55aa40428fa8895faff8c20cde
Source dataset
uspto-grants-1978_07
Patent number
US04101543

Reaction notes

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