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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157803Generated: November 2, 2026

Water → Benzyl 4-(3,3-diethoxypropanoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1157803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantEthyl 3,3-diethoxypropionateHCID 66389—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-(3,3-diethoxypropanoyl)piperazine-1-carboxylateHCID 2301429888%

Reaction Conditions

Temperature25 °C

Reaction Steps

Part A: To a solution of ethyl 3,3-diethoxypropionate (90% tech.) (5.28 g, 25 mmol) in 50 mL of THF was added 1.00 N sodium hydroxide in water (25.00 mL, 25 mmol), and the resulting mixture was stirred at 25° C. for 18 h. The mixture then was concentrated under vacuum to afford a residual white solid. This solid was dissolved in 50 mL of DMF. To the solution was added EDCI (5.75 g, 30.0 mmol), 1-hydroxybenzotriazole (4.56 g, 33.8 mmol), and benzyl piperazine-1-carboxylate (5.51 g, 25.0 mmol), and the resulting mixture was stirred at 25° C. for 24 h. The reaction mixture was concentrated under vacuum, and the residue was diluted with water. The aqueous mixture was extracted with ethyl acetate, and the combined extracts were washed aqueous sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Column chromatography on silica gel (elution: 10-40% ethyl acetate/chloroform) furnished 8.00 g (88%) of benzyl 4-(3,3-diethoxypropanoyl)piperazine-1-carboxylate as an oil; 1H NMR (500 MHz, CDCl3) δ 57.34 (m, 5H), 5.14 (s, 2H), 4.90 (t, 1H, J=5.5 Hz), 3.73-3.46 (m, 12H), 2.68 (d 2H, J=5.5 Hz), 1.19 (t, 6H, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807676B2
Source datasetuspto-grants-2010_10
ORD IDord-e1fa6f836f1a4a9c93f59a7d96d97505
Source noteuspto-grants-2010_10