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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896123Generated: October 25, 2026

Benzathine → Ethyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylate

https://huagongshe.com/reaction/1896123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzathineHCID 8793—
ReactantDiethyl bromomalonateHCID 69637—
SolventAcetonitrileHCID 6342—
SolventSodium HydroxideHCID 14798—
ProductEthyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylateHCID 15645950—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N,N′-dibenzylethylenediamine (14.12 mL, 60.2 mmol) in acetonitrile (100 mL) was added diethyl bromomalonate (5.14 mL, 30.1 mmol), and the mixture was heated with an oil bath at 90° C. (reflux) for 7 hours. The solvent was evaporated to provide a residue that was dissolved in 1 M NaOH (aqueous), and the mixture was extracted with ethyl acetate twice, dried over Na2SO4, and the solvent was evaporated. The crude mixture was purified by silica gel chromatography (Analogix IntelliFlash 280, SF40-150) eluting with 15%-30% ethyl acetate/hexanes to afford the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.38-7.20 (m, 10H), 4.54 (dd, J=15.0, 154.2, 2H), 4.20-4.10 (m, 2H), 4.03 (q, J=7.1, 1H), 3.96 (s, 1H), 3.61 (dd, J=13.5, 41.7, 2H), 3.27-3.14 (m, 2H), 3.05-2.95 (m, 1H), 2.60-2.52 (m, 1H), 1.23 (t, J=7.1, 3H); MS (ESI+) m/z 353.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518933B2
Source datasetuspto-grants-2013_08
ORD IDord-8952aed00abe4538a3e417ca54b074c9
Source noteuspto-grants-2013_08