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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367889Generated: October 25, 2026

Triethylamine → 1-Dimethylamino-piperidin-4-one oxime

https://huagongshe.com/reaction/2367889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant1-(Dimethylamino)-4-piperidinoneHCID 56737782—
SolventMethanolHCID 887—
Product1-Dimethylamino-piperidin-4-one oximeHCID 8667130468.3%

Reaction Conditions

Temperature37 °C

Reaction Steps

19.2 g 1-Dimethylamino-piperidin-4-one (prepared as described in Journal of Medicinal & Pharmaceutical Chemistry, 4, 423-36; 1961) and 30 g triethylamine are dissolved in 80 ml methanol. 18.8 g hydroxylamin hydrochloride is added in portions at ambient temperature. The internal temperature raises during the addition to 37° C. Then the mixture is heated to reflux for 3 hours, allowed to cool to room temperature, and then the solvent evaporated. The residue is partitioned between ethyl acetate and aqueous sodium bicarbonate. The organic layer is dried over sodium sulfate, and the solvent evaporated. Thus, 14.5 g 1-Dimethylamino-piperidin-4-one oxime is obtained. 1H-NMR (CDCl3): 8.10 ppm (s, broad, 1H), 2.75 ppm (m, 6H), 2.40 ppm (m, 2H), 2.40 ppm (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703165B2
Source datasetuspto-grants-2014_04
ORD IDord-26a3a45656db442682014dd6ec817748
Source noteuspto-grants-2014_04