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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979398Generated: October 30, 2026

O-Allylhydroxylamine → HCID 178460146, compound

https://huagongshe.com/reaction/979398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-AllylhydroxylamineHCID 420841—
Reactant5-(1-Benzofuran-2-yl)-2-butanoylcyclohexane-1,3-dioneHCID 20146016—
SolventEthanolHCID 702—
ProductHCID 178460146HCID 17846014692%

Reaction Steps

4.6 parts by weight of 2-butyryl-5-(benzo[b]fur-2-yl)-cyclohexane-1,3-dione, 1.2 parts by weight of allyloxyamine and 30 parts by volume of ethanol were stirred for 12 hours at room temperature. The solvent was distilled off under reduced pressure, the residue was taken up in 50 parts of dichloromethane, the solution was washed twice with water and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. 2-(1-Allyloxyaminobutylidene)-5-(benzo[b]fur-2-yl)-cyclohexane-1,3-dione was obtained as a viscous oil in a yield of 92% (compound no. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668275
Source datasetuspto-grants-1987_05
ORD IDord-dba2e8af06b941279c5fbfed16e16589
Source noteuspto-grants-1987_05