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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538662Generated: October 25, 2026

Thionyl Chloride → 1-Benzyl-2-(chloromethyl)piperidine

https://huagongshe.com/reaction/538662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(1-Benzylpiperidin-2-yl)methanolHCID 2735486—
SolventChloroformHCID 6212—
Product1-Benzyl-2-(chloromethyl)piperidineHCID 15015454—

Reaction Steps

To a stirred solution of compound 13 (3.6 g, 15.00 mmol) in chloroform (50 mL) was added thionyl chloride (1.34 mL) at 0° C. The reaction mixture was heated at reflux for 2 hours and then concentrated. The residue was dissolved in EtOAc and washed with saturated sodium bicarbonate solution, water and brine. The organic layer was dried over Na2SO4, filtered and concentrated. The crude material was purified by chromatography on 230-400 mesh silica gel eluting with 10% EtOAc-hexane to provide compound 14 as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865741B2
Source datasetuspto-grants-2014_10
ORD IDord-411c250c3a24456caa4a517d6cf6d979
Source noteuspto-grants-2014_10