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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614552Generated: October 30, 2026

Piperidine → Silperisone hydrochloride

https://huagongshe.com/reaction/1614552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantChloromethyl-dimethyl(4-fluorobenzyl)silaneHCID 15338764—
SolventO-XyleneHCID 7237—
ProductSilperisone hydrochlorideHCID 178567—

Reaction Steps

After adding 32.7 g of piperidine to a solution containing 32.5 g of chloromethyl-dimethyl-(4-fluorobenzyl)-silane in 40 ml of xylene, the reaction mixture is refluxed for 6 hours under stirring, then the precipitated piperidine hydrochloride is filtered at 20° C. and washed in 3 portions with a total of 60 ml of benzene. The filtration is combined with the benzene washings and washed in 3 portions with a total of 150 ml of water and the organic phase is dried over anhydrous magnesium sulfate. After filtering the drying agent, the filtrate is evaporated to solvent-free to give the crude name compound as an oily liquid in the base form in a yield of 40 g. This crude product is purified by distillation under reduced pressure to give the title compound in a yield of 36.8 g (92%) with a boiling point of 97°-98° C./0.5 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198446
Source datasetuspto-grants-1993_03
ORD IDord-427bd83639ef405eb68394b22be8e628
Source noteuspto-grants-1993_03