Ethanol → N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide
Reaction equation
[CH3:1][N:2]([CH3:11])[C:3](=[O:10])[C:4](=[N:8][OH:9])[C:5]([CH3:7])=O.C(O)C.Cl.[CH3:16][O:17][NH2:18]>N1C=CC=CC=1>[CH3:1][N:2]([CH3:11])[C:3](=[O:10])[C:4](=[N:8][OH:9])[C:5](=[N:18][O:17][CH3:16])[CH3:7]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 10 °C
Procedure
To a stirred mixture of 336 parts of N,N-dimethyl-2-hydroxyiminoacetoacetamide (a compound of Formula III), 1500 parts ethanol and 203 parts of methoxyamine hydrochloride were added dropwise 210 parts of pyridine over one-half hour while maintaining the reaction mixture at 10° C. by external cooling. The mixture was allowed to warm slowly to 25° C. and maintained at this temperature for 18 hours. Finally, it was stirred and refluxed for one-half hour. The solvent was removed under reduced pressure (15 mm.) at 40° C. bath temperature. Approximately 2000 parts of ice water were added, which caused the residue to solidify. The solid was filtered, washed twice with ice water, filtered, and dried. There was obtained 340 parts of N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide (a compound of Formula II), m.p. 144-147, which is of satisfactory quality for use as an intermediate. The product was, however, recrystallized from ethyl acetate, whereupon it melted at 146°-148°.
Workup
- temperatureto warm slowly to 25° C.
- temperaturemaintained at this temperature for 18 hours
- temperaturerefluxed for one-half hour
- customThe solvent was removed under reduced pressure (15 mm.) at 40° C. bath temperature
- additionApproximately 2000 parts of ice water were added
- filtrationThe solid was filtered
- washwashed twice with ice water
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-e804256bc6c342a28d4525441263ac60
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04151296
Reaction notes
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