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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469396Generated: October 30, 2026

Oxalyl chloride → HCID 21906247, compound

https://huagongshe.com/reaction/1469396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 21906247HCID 21906247—

Reaction Steps

To a solution of oxalyl chloride (8.72 ml, 17.45 mmol) in DCM (150 ml) was added 1-(tert-butoxy-carbonyl)piperidine-4-carboxylic acid (2 g, 8.72 mmol) at 0° C. Then a few drops of DMF were added. The mixture was stirred at room temperature for 2 h, washed with NH4Cl aqueous and brine. The organic layer was separated, dried (MgSO4) and concentrated. The resulting crude product was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006268B2
Source datasetuspto-grants-2015_04
ORD IDord-22ad9d1b73e146e1afeb665c8a27271d
Source noteuspto-grants-2015_04