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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245714Generated: October 26, 2026

Oxalyl chloride → 1-Methylpiperidine-4-carbonyl chloride hydrochloride

https://huagongshe.com/reaction/245714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-Piperidinecarboxylic acid, 1-methyl-, hydrochloride (1:1)HCID 2760043—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-Methylpiperidine-4-carbonyl chloride hydrochlorideHCID 21956506111.1%

Reaction Steps

To a suspension of 1-methyl-piperidine-4-carboxylic acid hydrochloride (11.36 mmol, 2.04 g) and N,N-dimethylformamide (0.129 mmol, 0.01 ml, 9.40 mg) in dichloromethane (10 ml) at 0° C. was added oxalyl chloride (14.76 mmol, 1.40 ml) drop wise. The cooling bath was removed and the reaction mixture stirred at room temperature for 20 hours. Then the reaction mixture was concentrated in vacuo to give 1-methylpiperidine-4-carbonyl chloride hydrochloride (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658794B2
Source datasetuspto-grants-2014_02
ORD IDord-5c63cbcfa90a49bcbd1a3c66ee2477c2
Source noteuspto-grants-2014_02