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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606939Generated: October 30, 2026

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

https://huagongshe.com/reaction/1606939

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 numberUS04863926
Source datasetuspto-grants-1989_09
ORD IDord-04395c6aa7d7415380eb349b5531032f
Source noteuspto-grants-1989_09