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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17865Generated: October 25, 2026

Oxalyl chloride → benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/17865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productbenzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylateHCID 2776575—

Reaction Steps

To an ice cooled methylene chloride solution of 1-[(Benzyloxy)carbonyl]piperidine-3-carboxylic acid (512 mg, 1.95 mmol) under nitrogen was added oxalyl chloride (0.185 mL, 1.95 mmol) and a few drops N,N-dimethylformamide. The reaction flask was warmed slowly to room temperature and after 2 hours the solvent was removed in vacuo. Toluene was added and removed in vacuo (2×) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741322B2
Source datasetuspto-grants-2010_06
ORD IDord-41058c22e6b04ecb9835b0c445873296
Source noteuspto-grants-2010_06