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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387322Generated: October 31, 2026

Benzaldehyde → 4-Aminomethyl-1-N-Cbz-piperidine

https://huagongshe.com/reaction/1387322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-(Aminomethyl)piperidineHCID 23527—
ReactantPotassium bisulfateHCID 516920—
SolventTolueneHCID 1140—
Product4-Aminomethyl-1-N-Cbz-piperidineHCID 2195549991%

Reaction Conditions

Temperature0 °C

Reaction Steps

22.2 g(0.2 mol) of 4-aminomethylpiperidine was dissolved in 250 ml of toluene and 21.2 g(0.2 mol) of benzaldehyde was added thereto. The reaction mixture was refluxed for 3 hours with Dean-stack to remove water, and then cooled down to 0° C. 34.2 g(0.2 mol) of benzylchloroformate was added slowly thereto while stirring. The mixture was stirred at room temperature for 3 hours and 220 ml of 1N aqueous KHSO4 solution was added thereto. The mixture was extracted three times with 200 ml of diethylether, and the aqueous layer was basified with 1N aqueous sodium hydroxide solution. The aqueous solution was saturated with sodium chloride. The aqueous layer was extracted three times with 100 ml of dichloromethane, dried over anhydrous magnesium sulfate and distilled under reduced pressure to give 38 g(Yield 91%, Molecular weight 248) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268363B1
Source datasetuspto-grants-2001_07
ORD IDord-4f531819aea5484797e05990c24a848e
Source noteuspto-grants-2001_07