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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649633Generated: November 1, 2026

Triethylamine → HCID 136056433, compound

https://huagongshe.com/reaction/1649633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-Allylhydroxylamine hydrochlorideHCID 3084724—
Reactant2-Butyryl-3-hydroxy-4-(4-methoxyphenyl)cyclohex-2-ene-1-oneHCID 19854189—
SolventEthanolHCID 702—
ProductHCID 136056433HCID 13605643366.6%

Reaction Steps

Triethylamine (1.2 g) was added to a solution of 2-butyryl-3-hydroxy-4-(4-methoxyphenyl)cyclohex-2-e-n-1-one (2.9 g) and O-allylhydroxylamine hydrochloride (1.2 g) in absolute ethanol (50 ml) at ambient temperature. After stirring overnight at this temperature, the ethanol was evaporated in vacuo, water was added to the residue and the aqueous solution was extracted with methylene chloride. The organic extracts were dried over anhydrous magnesium sulphate and then evaporated in vacuo. The residue was chromatographed on a silica gel column using 10% Et2O--CH2Cl2 as eluant to give the title compound (2.3 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921524
Source datasetuspto-grants-1990_05
ORD IDord-8b953e3462cd479cb7bf9f1310307946
Source noteuspto-grants-1990_05