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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757439Generated: October 29, 2026

3-Methylpiperidine → HCID 21154844, compound

https://huagongshe.com/reaction/1757439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylpiperidineHCID 79081—
ReactantHCID 19388019HCID 19388019—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 21154844HCID 21154844—

Reaction Steps

18.85 g (0.10 mol) of 4-chloro-l-(2-thienyl)butanone are run, over a periodof 30 min, into a solution, maintained at 100° C., of 21.8 g (0.22 mol) of 3-methylpiperidine in 35 ml of toluene, and the mixture is heated to reflux for 2 hours. The reaction medium is diluted with ethyl ether andthe mixture is washed with water. The organic phase is extracted with dilute hydrochloric acid solution which, after alkalinisation with sodium hydroxide, is in turn extracted with ethyl ether. The organic phase is dried over dry sodium sulphate and treated with a solution of hydrogen chloride in isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446060
Source datasetuspto-grants-1995_08
ORD IDord-86773fd17b274149a38ae049fd4e9af4
Source noteuspto-grants-1995_08