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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497645Generated: October 29, 2026

4-Piperidinecarboxamide → benzyl 4-(aminocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/1497645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidinecarboxamideHCID 3772—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Productbenzyl 4-(aminocarbonyl)tetrahydro-1(2H)-pyridinecarboxylateHCID 277613176%

Reaction Steps

To a solution of piperidine-4-carboxamide (5 g, 39 mmol) and benzylchloroformate (5.54 mL, 39 mmol) in a mixture of water (30 mL) and acetone (40 mL), NaOH 1N (39 mL, 39 mmol) was added dropwise, while maintaining the pH between 6 and 8. The mixture was stirred at r.t. for 3 h; then acetone was evaporated and the resulting precipitate filtered and dried at 70° C. under reduced pressure, giving 7.75 g of benzyl-4-carbamoylpiperidine-1-carboxylate (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199979B2
Source datasetuspto-grants-2015_12
ORD IDord-7d8dfbdbecc44e4f9aa4d905818ba5ff
Source noteuspto-grants-2015_12