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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830724Generated: October 26, 2026

Benzaldehyde → N-benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1830724

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>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. 1H-NMR (400 MHz, CDCl3) δ7.85 (m, 5H), 5.45 (s, 1H), 5.34 (s, 1H), 3.5 (s, 2H), 2.93 (d, J=10.96 Hz, 2H), 2.16 (t, J=12.13 Hz, 1H), 2.01 (t, J=11.74 Hz, 2H), 1.87 (d, J=12.52 Hz, 2H), 1.76 (q, J=12.52 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067506B2
Source datasetuspto-grants-2006_06
ORD IDord-b6e5831158794da89645e89ab4cd8afb
Source noteuspto-grants-2006_06