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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231307Generated: October 31, 2026

Acetic Acid → (E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamide

https://huagongshe.com/reaction/2231307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiazomethaneHCID 9550—
Reactant(E)-4-ethyl-2-hydroxyimino-5-nitro-3-hexenamideHCID 86742405—
SolventMethanolHCID 887—
Product(E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamideHCID 86742404—

Reaction Steps

To (E)-4-ethyl-2-hydroxyimino-5-nitro-3-hexenamide (37 mg) in methanol (5 ml) was added excess etheral diazomethane at -20° C. The resulting mixture was allowed to stand at 0° C. for an hour and then acetic acid was added thereto until the yellow color of the solution was discharged. The resulting reaction mixture was evaporated under reduced pressure to give an oil which was purified by preparative thin layer chromatography, developing with chloroform containing 5% methanol to give (E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamide (21.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782088
Source datasetuspto-grants-1988_11
ORD IDord-facec02093c7462cbc45ace71390c8b7
Source noteuspto-grants-1988_11