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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387325Generated: November 1, 2026

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

https://huagongshe.com/reaction/1387325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-(Aminomethyl)piperidineHCID 23527—
ReactantPotassiumHCID 5462222—
SolventTolueneHCID 1140—
Product4-Aminomethyl-1-N-Cbz-piperidineHCID 2195549991%

Reaction Conditions

Temperature0 °C

Reaction Steps

22.2 g(0.2 mol) of 4-aminomethyl-piperidine was dissolved in 250 ml of toluene and then 21.2 g(0.2 mol) of benzaldehyde was added thereto. The mixture was refluxed for 3 hours with Dean-stack and cooled down to 0° C., and then 34.2 g(0.2 mol) of benzylchloroformate was added thereto while stirring. After the mixture was stirred for 3 hours, 1N aqueous potassium hydrosulfate solution(220 ml) was added thereto at room temperature. The mixture was extracted three times with 200 ml of diethylether, and then the aqueous layer was basified with sodium hydroxide. The aqueous solution was saturated with sodium chloride and extracted three times with 100 ml of dichloromethane. The organic solution was dried over magnesium sulfate and distilled under reduced pressure to obtain 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-e7830c2010ac4d12934b885c28d36a91
Source noteuspto-grants-2001_07