Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304575Generated: October 31, 2026

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

https://huagongshe.com/reaction/2304575

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-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 dropwise thereto while stirring. After the mixture was stirred for 3 hours, 1N aqueous potassium hydrogen sulfate solution(220 ml) was added thereto at room temperature. The mixture was extracted three times with 200 mg 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 numberUS06436960B1
Source datasetuspto-grants-2002_08
ORD IDord-c4f4bd2a53ae4661a9b5fbda6c39bc07
Source noteuspto-grants-2002_08