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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26708Generated: October 26, 2026

Ethanol → N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide

https://huagongshe.com/reaction/26708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 178468379HCID 178468379—
SolventPyridineHCID 1049—
ProductN,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramideHCID 136099002—

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151296
Source datasetuspto-grants-1979_04
ORD IDord-e804256bc6c342a28d4525441263ac60
Source noteuspto-grants-1979_04