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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71776Generated: October 25, 2026

Oxalyl chloride → Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/71776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270101.8%

Reaction Steps

Piperidine-1,4-dicarboxylic acid monobenzyl ester (40.2 g, 0.15 mol) in dichloromethane (300 mL) was treated with oxalyl chloride (100 g, 0.79 mol). The reaction mixture was stirred at ambient temperature for 4 hours and the mixture was concentrated to afford crude 4-chlorocarbonyl-piperidine-1-carboxylic acid benzyl ester (43 g), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822430B2
Source datasetuspto-grants-2014_09
ORD IDord-a81812e566a8409c8e53a751d6d3ed8c
Source noteuspto-grants-2014_09