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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511600Generated: November 4, 2026

Sodium borohydride → Ethyl 3-[(2-furylmethyl)amino]propanoate

https://huagongshe.com/reaction/1511600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3-[(furan-2-ylmethylene)amino]propanoateHCID 68410140—
SolventEthanolHCID 702—
ProductEthyl 3-[(2-furylmethyl)amino]propanoateHCID 273642655.7%

Reaction Steps

Ethyl 3-[(furan-2-ylmethylene)amino]propionate (19.2 g) prepared in the step 1 was dissolved in 200 mL of dry ethanol, 4.46 g of sodium borohydride was slowly added thereto little by little at room temperature and the mixture was stirred overnight at room temperature. The solvent was evaporated in vacuo from the reaction and the residue was poured over 300 mL of 10% aqueous solution of acetic acid. The resulting aqueous solution was washed with diethyl ether, neutralized with 10% aqueous ammonia and subjected to extraction with diethyl ether. The organic layer was washed with water and a saturated solution of sodium chloride successively and dried over anhydrous magnesium sulfate and the solvent was evaporated in vacuo therefrom to give 10.8 g of the objective compound as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217031B2
Source datasetuspto-grants-2012_07
ORD IDord-bc65e3dbd9d54b10a87ce2a75e563efa
Source noteuspto-grants-2012_07