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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432830Generated: October 25, 2026

Benzaldehyde → (S)-ethyl 1-benzyl-3-piperidinecarboxylate

https://huagongshe.com/reaction/432830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantEthyl (3S)-piperidine-3-carboxylateHCID 187784—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(S)-ethyl 1-benzyl-3-piperidinecarboxylateHCID 76347939.5%

Reaction Steps

(S)-ethyl nipecotate (309.1 mg; 1.97 mmol) was dissolved in anhydrous methanol (8 ml) and commercially available benzaldehyde (200 μl; 1.97 mmol) was added, followed by sodium cyanoborohydride (234 mg; 3.72 mmol). This mixture was allowed to stir at ambient temperature for 23 hours and was then diluted with dichloromethane. The dichloromethane was washed with water, then washed with saturated sodium chloride solution, dried with anhydrous potassium carbonate, and evaporated under reduced pressure at ambient temperature. The crude product was purified by chromatography on silica eluting with 50% ethyl acetate/50% hexane, giving (S)-ethyl 1-benzyl-3-piperidinecarboxylate (192.7 mg) as a colorless oil. MS mi/z (positive ion) 248 (MH+; 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664271B1
Source datasetuspto-grants-2003_12
ORD IDord-472ed590b85742f8a3342adc795a622e
Source noteuspto-grants-2003_12