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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80506Generated: October 25, 2026

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

https://huagongshe.com/reaction/80506

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 1M 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, 100H), 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 numberUS08846663B2
Source datasetuspto-grants-2014_09
ORD IDord-db0d9fb1250f40c7b3788303d58a5c1a
Source noteuspto-grants-2014_09