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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868229Generated: October 30, 2026

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

https://huagongshe.com/reaction/868229

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 numberUS04778804
Source datasetuspto-grants-1988_10
ORD IDord-d26d0d9c34ba449291067e49f637a27a
Source noteuspto-grants-1988_10