Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552326Generated: October 31, 2026

Triethylamine → 1-(2-Ethylbutyryl)piperidin-4-one

https://huagongshe.com/reaction/552326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Ethylbutyryl chlorideHCID 75954—
ReactantPiperidin-2-one--hydrogen chloride (1/1)HCID 20088740—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(2-Ethylbutyryl)piperidin-4-oneHCID 24710387—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Triethylamine (5.8 g, 57.3 mmol) and a catalytic amount of DMAP were added to a solution of piperidone hydrochloride (4.0 g, 26 mmol) in CH2Cl2 (20 ml). After cooling to −10° C., 2-ethylbutyryl chloride (3.9 g, 28.6 mmol) dissolved in CH2Cl2 (10 ml) was slowly added and the mixture was stirred at RT for 16 h. 5M potassium hydroxide solution (25 ml) was added to the suspension, the organic phase was separated off and the aqueous phase was extracted with CH2Cl2 (3×10 ml). After drying of the combined organic phases over Na2SO4, filtration and removal of the solvent, the product 1-(2-ethylbutyryl)piperidin-4-one was obtained in a yield of 4.3 g (84% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-d8be83b15251499db356120b356c60bd
Source noteuspto-grants-2011_05