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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239108Generated: October 29, 2026

Hydrochloric Acid → 1-benzyl-N-[(2-nitrophenyl)methyl]piperidin-4-amine

https://huagongshe.com/reaction/239108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-benzyl-N-[(2-nitrophenyl)methyl]piperidin-4-amineHCID 484876299.8%

Reaction Steps

5955 g 2-nitrobenzaldehyde was suspended in 10 L methanol under nitrogen atmosphere and 7500 g 4-amino-1-benzyl-piperadine in 5 L methanol was added over 30 min. The reaction was stirred 1 h at RT. The reaction mixture was cooled to 0° C. and a cold solution of 1044 g sodium borohydride in 6425 mL water was added at a rate to keep the temperature below 10° C. After 1 h stirring at 0° C. and 1 h at RT the reaction was cooled again to 0° C. and aqueous 4 mol/L hydrochlorid acid was added. Then the reaction mixture was stirred at RT for 30 min and cooled again to 0-10° C. Aqueous 5 mol/L sodium hydroxide solution was added until pH=14 and the reaction was extracted with tert-butyl methylether. The organic layer was washed with water and saturated sodium chloride solution and the solvent was evaporated. The residue was dissolved in toluol, filtered and concentrated again to yield 12.8 kg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642774B2
Source datasetuspto-grants-2014_02
ORD IDord-e09f06aff0cc4ca0aef95b2fcd84aae2
Source noteuspto-grants-2014_02