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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570015Generated: October 26, 2026

Ethanol → HCID 13769871, compound

https://huagongshe.com/reaction/570015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Benzylpiperazine-1-carboxamidine hemisulfateHCID 2756652—
ReactantSodiumHCID 5360545—
ReactantEthoxymethylene oxalacetic acid ethyl esterHCID 54255144—
ProductHCID 13769871HCID 1376987196%

Reaction Steps

To absolute ethanol with 0.91 g of sodium dissolved therein, 11.5 g of 1-amidino-4-benzylpiperazine sulfate was added. The resultant mixture was stirred at room temperature for 30 minutes, to which 8.8 g of ethyl ethoxymethyleneoxaloacetate [synthesized by the process described in J. Am. Chem. Soc., 73, 3684 (1951)] was added. After allowing them to react at room temperature for 2 days, the reaction was caused to proceed further for 1 hour while heating the reaction mixture under reflux. After cooling the reaction mixture to room temperature, ethanol was distilled off under reduced pressure and the residue was dissolved in a mixture of water and ethyl acetate. After separation of the water layer, the ethyl acetate layer was washed with water and then with saturated saline. After drying the ethyl acetate layer with magnesium sulfate, ethyl acetate was distilled off under reduced pressure to obtain 13.7 g of the above-identified compound as light brown crystals (yield: 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734418
Source datasetuspto-grants-1988_03
ORD IDord-a01e75ffd96d4cdf86e410cb6dbd5ed1
Source noteuspto-grants-1988_03