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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906697Generated: November 1, 2026

O-Allylhydroxylamine → HCID 178460148, compound

https://huagongshe.com/reaction/1906697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-AllylhydroxylamineHCID 420841—
ReactantHCID 20210168HCID 20210168—
SolventMethanolHCID 887—
ProductHCID 178460148HCID 178460148—

Reaction Steps

14.0 parts by weight of 2-butyryl-5-(tetrahydropyran-4-yl)-cyclohexane-1,3-dione and 4.2 parts by weight of allyloxyamine in 100 parts by volume of methanol are stirred for 16 hours at room temperature. The solvent is distilled off under reduced pressure, the residue is dissolved in dichloromethane, the solution is then washed with 5% strength hydrochloric acid and water and dried over sodium sulfate, and the solvent is stripped off under reduced pressure to give 12.9 parts by weight of 2-(1-allyloxyamino-n-butylidene)-5-(tetrahydropyran-4-yl)cyclohexane-1,3-dione in the form of a solid (active ingredient No. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654073
Source datasetuspto-grants-1987_03
ORD IDord-0161891900f44d98b694e9a2f17e0390
Source noteuspto-grants-1987_03