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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096002Generated: October 31, 2026

Chloroacetyl chloride → 1-(2-chloroacetyl)-N-(1,1-dimethylethyl)-4-piperidinecarboxamide

https://huagongshe.com/reaction/2096002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
ReactantN-tert-butylpiperidine-4-carboxamideHCID 7175833—
SolventDichloromethaneHCID 6344—
Product1-(2-chloroacetyl)-N-(1,1-dimethylethyl)-4-piperidinecarboxamideHCID 6874331071.1%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A solution of N-(1,1-dimethylethyl)-4-piperidinecarboxamide (201 g, 1.0 mol) in dichloromethane (1 L) was cooled under nitrogen to −5° C., and chloroacetyl chloride (124 g, 1.1 mol) in 300 mL of dichloromethane was added dropwise over 30 minutes while maintaining the reaction mixture at 0 to 5° C. Then 20% aqueous potassium carbonate solution (450 g, 0.65 mol) was added dropwise over 30 minutes while keeping reaction temperature between 0 and 5° C. The reaction mixture was stirred for an additional 30 minutes at 0° C., and then allowed to warm to room temperature. The layers were separated, and the aqueous layer was extracted with dichloromethane (200 mL). The combined dichloromethane layers were concentrated under reduced pressure to yield a solid, which was triturated with 400 mL of hexanes. The slurry was filtered, and the filter cake was washed with 100 mL of hexanes and dried in a vacuum oven overnight at 50° C. to give 185.5 g of 1-(2-chloroacetyl)-N-(1,1-dimethylethyl)-4-piperidinecarboxamide as a solid, melting at 140.5-141.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449898B2
Source datasetuspto-grants-2013_05
ORD IDord-126d5bf67d84461f8713badaf3c058a4
Source noteuspto-grants-2013_05