HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971894Generated: October 26, 2026
Ethanol → N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide
https://huagongshe.com/reaction/971894
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 178468379 | HCID 178468379 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide | HCID 136099002 | — |
Reaction Steps
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°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04161591 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-12e1a79bfad14c8a9b9a04cbb098cbad |
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| Source note | uspto-grants-1979_07 |
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