Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840000Generated: October 30, 2026

Ammonia → 2,2,6,6-Tetramethyl-3-(prop-2-en-1-yl)piperidin-4-one

https://huagongshe.com/reaction/840000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant5-Allyl-1,2,5,6-tetrahydro-2,2,6,6-tetramethyl-4-piperidinopyridineHCID 21330385—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2,2,6,6-Tetramethyl-3-(prop-2-en-1-yl)piperidin-4-oneHCID 21330490—

Reaction Steps

1.46 g of the 5-allyl-1,2,5,6-tetrahydro-2,2,6,6-tetramethyl-4-piperidinopyridine thus obtained were dissolved in a mixture of 3 ml of acetic acid, 1.5 g of sodium acetate and 3 ml of water, and the solution was allowed to stand overnight. To the solution were then added 6.0 g of sodium bicarbonate and 3 ml of concentrated aqueous ammonia; the solution was then extracted with hexane. The hexane extract was dried over magnesium sulphate and then treated with charcoal giving, after removal of the hexane, 0.91 g of 3-allyl-2,2,6,6-tetramethyl-4-piperidone. On thin layer chromatography using a 0.25 mm thick layer of alumina and a mixture of benzene, hexane, ethyl acetate and triethylamine (2 : 2 : 1 : 0.5 by volume) as developing solvent, the compound showed a single spot having an Rf value of 0.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097587
Source datasetuspto-grants-1978_06
ORD IDord-dcb4d7d6b64346b3abef2d6038d717d5
Source noteuspto-grants-1978_06