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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzathine | HCID 8793 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Ethyl 1,4-dibenzyl-3-oxopiperazine-2-carboxylate | HCID 15645950 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518933B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-8952aed00abe4538a3e417ca54b074c9 |
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| Source note | uspto-grants-2013_08 |
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