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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604342Generated: October 25, 2026

Aminoethylpiperazine → Benzyl (4,4-diethoxybutyl)carbamate

https://huagongshe.com/reaction/1604342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoethylpiperazineHCID 8795—
ReactantBenzyl chloroformateHCID 10387—
Reactant4,4-DiethoxybutylamineHCID 80672—
SolventDichloromethaneHCID 6344—
SolventSodium CarbonateHCID 10340—
ProductBenzyl (4,4-diethoxybutyl)carbamateHCID 11471964—

Reaction Steps

Three portions of benzyl chloroformate (260 ml) in dichloromethane (170 ml) were added sequentially over 1 h 40 min to a vigorously stirred mixture of 4-aminobutyraldehyde diethyl acetal (910 ml) in dichloromethane (3 l) and aqueous sodium carbonate (1M, 3 l). Stirring was continued for 50 min until gas evolution ceased. N-(2-aminoethyl)piperazine (40 ml) was added and stirring was continued for 1 h 15 min. The layers were separated and the organic layer was washed with aqueous citric acid (1M, 3.8 l) and saturated aqueous sodium bicarbonate (2 l), dried (MgSO4), filtered and concentrated in vacuo to give the title compound as a yellow oil (1.6 kg). T.l.c. (Ether) Rf 0.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994344
Source datasetuspto-grants-1999_11
ORD IDord-004e30bcc97e4b119b8ce29e35568eaf
Source noteuspto-grants-1999_11