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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401974Generated: October 27, 2026

Benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate → HCID 49760816, compound

https://huagongshe.com/reaction/1401974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylateHCID 59436481—
SolventHydrochloric AcidHCID 313—
ProductHCID 49760816HCID 4976081689%

Reaction Steps

A solution of benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate (Preparation 234, 73 g, 0.2 mol) in concentrated hydrochloric acid (200 ml) was refluxed with stirring for 2 hours before concentrating in vacuo. Water (100 ml), sodium hydroxide (10 M aqueous solution, 20 ml) and chloroform (200 ml) were added to the residue. The aqueous layer was extracted with chloroform (2×200 ml). The combined organic layers were washed with water (200 ml), saturated aqueous sodium chloride solution (200 ml), dried over sodium sulphate, filtered through silica gel (100 g, 40/63 μm) and evaporated in vacuo to afford the title compound as white crystals, 40 g, 89% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-0e91d032ad2a4f7ab31109673caac2c9
Source noteuspto-grants-2014_12