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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821742Generated: October 26, 2026

Benzaldehyde → N-benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1821742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant4-PiperidinecarboxamideHCID 3772—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-benzylpiperidine-4-carboxamideHCID 386806451.7%

Reaction Steps

To a suspension of isonipecotamide (12.3 g, 96 mmol) in 200 mL of dichloromethane, was added, benzaldehyde (10.6 g, 100 mmol) and sodium triacetoxyborohydride (29.7 gm, 140 mmol) and the mixture was stirred at room temperature for 5 days. The thick white mixture was diluted with 100 mL water and extracted with EtOAc (2×20 mL) The aqueous phase was basified with 1N NaOH to pH 22 12. The resulting white precipitate was collected by suction filtration. The white solid was subsequently taken up in 50 mL of EtOAc, and was washed with 20 mL of brine, then dried (MgSO4), filtered and concentrated to give 10.84 g (50%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608618B2
Source datasetuspto-grants-2009_10
ORD IDord-9f6ced7b52864182937ca60b840dfc01
Source noteuspto-grants-2009_10