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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3-[(furan-2-ylmethylene)amino]propanoate | HCID 68410140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-[(2-furylmethyl)amino]propanoate | HCID 2736426 | 55.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217031B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-bc65e3dbd9d54b10a87ce2a75e563efa |
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| Source note | uspto-grants-2012_07 |
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