p-Toluenesulfonic acid → N,N-dimethyl-2-hydroxyimino-3-(4-methoxyphenylimino)butyramide
Reaction equation
[CH3:1][N:2]([CH3:11])[C:3](=[O:10])[C:4](=[N:8][OH:9])[C:5]([CH3:7])=O.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:1][N:2]([CH3:11])[C:3](=[O:10])[C:4](=[N:8][OH:9])[C:5](=[N:20][C:17]1[CH:18]=[CH:19][C:14]([O:13][CH3:12])=[CH:15][CH:16]=1)[CH3:7]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
a mixture of 142 parts of N,N-dimethyl-2-hydroxyiminoacetoacetamide (a compound of Formula III), 1200 parts of toluene, 123 parts of p-anisidine and 1 part of p-toluenesulfonic acid was refluxed overnight in a flask fitted with a Dean-Stark distilling trap and water condenser. Eighteen parts of water were removed in this manner. On cooling, a heavy slurry of solid product precipitated. This was filtered and washed with butyl chloride thereby providing a product which melted at 201.5°-203° C. Recrystallization from acetonitrile gave 151 parts of N,N-dimethyl-2-hydroxyimino-3-(4-methoxyphenylimino)butyramide (a compound of Formula II) as a yellow solid, m.p. 204°-205.5° C.
Workup
- temperaturewas refluxed overnight in a flask
- customfitted with a Dean-Stark
- distillationdistilling trap and water condenser
- customEighteen parts of water were removed in this manner
- temperatureOn cooling
- customa heavy slurry of solid product precipitated
- filtrationThis was filtered
- washwashed with butyl chloride
- customthereby providing a product which melted at 201.5°-203° C
- customRecrystallization from acetonitrile
Sources & evidence
- ORD record
- ord-4d1d0f4823fa48139ec5a9f984cb74bd
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04151296
Reaction notes
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