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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307165Generated: November 2, 2026

Triethylamine → (+/-)-3-(2,4-Dihydroxyphenyl)cyclopentanone Oxime

https://huagongshe.com/reaction/2307165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(+/-)-3-(2,4-Dihydroxyphenyl)cyclopentanoneHCID 22337821—
SolventEthanolHCID 702—
Product(+/-)-3-(2,4-Dihydroxyphenyl)cyclopentanone OximeHCID 86586325—

Reaction Steps

(±)-3-(2,4-Dihydroxyphenyl)cyclopentanone (5 mg), hydroxylamine hydrochloride (2.7 mg) and triethylamine (5.4 uM) were heated in EtOH (4 ml) under reflux for 3 hr. The reaction mixture was partitioned between ethyl acetate (20 ml) and water (20 ml). The aqueous phase was extracted with ethyl acetate (10 ml), and the combined organic phases were washed with brine (10 ml), dried over magnesium sulfate, and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 4:1 v/v) to furnish the title compound as a white solid and a mixture of isomers (3.8 mg, 71%). δH (d4-MeOH) 1.80-1.93 (1H, overlapping m), 2.05-2.20 (0.5H, m), 2.39-2.55 (3H, overlapping m), 2.68-2.74 (1H, overlapping m), 2.94 (0.5H, br dd), 6.26-6.33 (2H, overlapping m), 6.94 (0.5H, d), 6.96 (0.5H, d); m/z (ES−) 266 ((M+60)−1)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828460B2
Source datasetuspto-grants-2004_12
ORD IDord-0d4fe1b1121d4d6aabd94ddd0c67f235
Source noteuspto-grants-2004_12