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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391228Generated: November 3, 2026

Hydrochloric Acid → 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one

https://huagongshe.com/reaction/1391228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium BromideHCID 25514—
Reactant2,4,6-Triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidineHCID 20527890—
SolventMethanolHCID 887—
Product2,6-Diethyl-2,3,6-trimethylpiperidin-4-oneHCID 22182213—

Reaction Steps

19.6 g of 2,4,6-triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine and 0.4 g of ammonium bromide were added to 200 ml of methanol. To the mixture were added dropwise 10 g of a 37% aqueous hydrochloric acid solution at 10° C., with stirring. When the addition was complete, the whole mixture was stirred at room temperature for 4 hours, after which 20 ml of 18% aqueous hydrochloric acid were then added. The mixture was then heated at 30°-40° C. for 7 hours and allowed to stand overnight at room temperature. The resulting mixture was made alkaline by addition of a 40% aqueous solution of potassium carbonate and, after evaporating off the methanol under reduced pressure, the mixture was extracted with diethyl ether. The ethereal extract was dried over potassium carbonate, after which the diethyl ether was removed. The residue was then distilled under reduced pressure, giving 15.1 g of the title compound as an oil boiling at 91°-93° C./2.0 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04141883
Source datasetuspto-grants-1979_02
ORD IDord-779d405a13e24094a88e12e748ee8b2d
Source noteuspto-grants-1979_02