Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965537Generated: October 30, 2026

Benzaldehyde → Benzyl 4-(2-aminoethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/965537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantAminoethylpiperazineHCID 8795—
ProductBenzyl 4-(2-aminoethyl)piperazine-1-carboxylateHCID 10890711—

Reaction Steps

8.21 g of benzaldehyde are added to a solution of 10 g of 1-(2-aminoethyl)piperazine in 125 ml of toluene and the mixture is refluxed for 3 hours, the water formed being removed by means of a Dean-Stark apparatus. The reaction mixture is concentrated under vacuum, the residue is taken up with 100 ml of DCM, 13.45 ml of DIPEA are added and 11.03 ml of benzyl chloroformate are added dropwise. The reaction mixture is stirred overnight at RT and concentrated under vacuum. The residue is taken up with a saturated solution of potassium hydrogensulfate and stirred vigorously for 4 hours at RT. The aqueous phase is washed with ether, rendered alkaline to pH 9-10 by the addition of concentrated NaOH, saturated by the addition of NaCl and extracted with chloroform, the organic phase is dried over sodium sulfate and the solvent is evaporated off under vacuum to give 18.78 g of the expected product, which is used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773612
Source datasetuspto-grants-1998_06
ORD IDord-ce296651c34f410a9e2e13d0dc4aef8a
Source noteuspto-grants-1998_06