Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419457Generated: October 26, 2026

Hydrochloric Acid → HCID 20315688, compound

https://huagongshe.com/reaction/2419457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
Reactant4-BenzhydrylpiperidineHCID 88278—
Reactant1-(2-Piperidinoethyl)-4-(diphenylmethyl)piperidineHCID 20315689—
SolventEthanolHCID 702—
ProductHCID 20315688HCID 20315688—

Reaction Steps

Following Scheme I, 18.1 parts of 4-diphenylmethylpiperidine (U.S. Pat. No. 3,806,526) 13.6 parts of 2-chloroethylpiperidine hydrochloride and 16 parts of sodium carbonate are placed in 250 parts of aqueous 95% ethanol and heated at reflux for 5 hours with stirring. The ethanol is removed to provide an oil which is 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine. This oil is dissolved in anhydrous ethanol and 2 equivalents of hydrochloric acid gas are added to provide 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine dihydrochloride, melting at 330° C. The anhydrous ethanol solution of 1-(2-piperidinoethyl)-4-(diphenylmethyl)piperidine is reacted with 1.5 equivalents of oxalic acid to provide the oxalic acid salt. In a similar manner other previously mentioned pharmaceutically acceptable salts are formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105849
Source datasetuspto-grants-1978_08
ORD IDord-dd096a6207734e7b9b1dcffdf792d7c1
Source noteuspto-grants-1978_08