p-Toluenesulfonic acid → N,N-dimethyl-2-hydroxyimino-3-(4-methoxyphenylimino)butyramide

HRID 26709Notes

Reaction equation

HRID 26709 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

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

  1. temperaturewas refluxed overnight in a flask
  2. customfitted with a Dean-Stark
  3. distillationdistilling trap and water condenser
  4. customEighteen parts of water were removed in this manner
  5. temperatureOn cooling
  6. customa heavy slurry of solid product precipitated
  7. filtrationThis was filtered
  8. washwashed with butyl chloride
  9. customthereby providing a product which melted at 201.5°-203° C
  10. customRecrystallization from acetonitrile

Sources & evidence

ORD record
ord-4d1d0f4823fa48139ec5a9f984cb74bd
Source dataset
uspto-grants-1979_04
Patent number
US04151296

Reaction notes

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