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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023018Generated: October 25, 2026

Chloroacetyl chloride → 1-(2-Chloroacetyl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1023018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactant4-CyanopiperidineHCID 138223—
SolventDichloromethaneHCID 6344—
Product1-(2-Chloroacetyl)piperidine-4-carbonitrileHCID 6747009792.9%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A mixture of 4-piperidinecarbonitrile (200 g, 1.80 mol) and 40% aqueous potassium carbonate solution (342 g, 0.99 mol) in dichloromethane (1 L) was cooled to −10° C., and a solution of chloroacetyl chloride (210 g, 1.86 mol) in dichloromethane (300 mL) was added over about 75 minutes while maintaining the reaction mixture at −10 to 0° C. After the addition was complete, the reaction mixture was separated, the upper aqueous phase was extracted with dichloromethane (2×300 mL), and the combined organic phases were concentrated under reduced pressure to give 312 g of the title compound as a liquid which slowly crystallized on standing. This compound was of sufficient purity to use in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722678B2
Source datasetuspto-grants-2014_05
ORD IDord-7e23b385b08f45b3840ed4d253a51158
Source noteuspto-grants-2014_05