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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164371Generated: October 27, 2026

O-Allylhydroxylamine → 2-[1-(Allyloxyimino)butyl]-5-[4-(ethylthio)carbonylphenyl]-3-hydroxy-2-cyclohexen-1-one

https://huagongshe.com/reaction/2164371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-AllylhydroxylamineHCID 420841—
ReactantHCID 178450327HCID 178450327—
SolventTetrahydrofuranHCID 8028—
Product2-[1-(Allyloxyimino)butyl]-5-[4-(ethylthio)carbonylphenyl]-3-hydroxy-2-cyclohexen-1-oneHCID 136042636—

Reaction Steps

Into 20 ml og tetrahydrofuran was dissolved 2 g of 2-butyryl-5-[4-(ethylthio)carbonylphenyl]-3-hydroxy-2-cyclohexen-1-one and to the solution was added 0.8 g of allyloxyamine. The mixture was kept for 15 hours at room temperature and the solvent was distilled off from it under reduced pressure. Then, the residue was recrystallized with mixture of benzene-ligroin and 0.8 g of colorless objective crystals having a melting point of 72°-75° C. was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504305
Source datasetuspto-grants-1985_03
ORD IDord-b0cfa799dce6495ab6481f1dceda76c2
Source noteuspto-grants-1985_03