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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884124Generated: October 30, 2026

Sodium borohydride → HCID 68524228, compound

https://huagongshe.com/reaction/884124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68527540HCID 68527540—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 68524228HCID 68524228—

Reaction Steps

To a solution of ethyl 3-[4-(5-nitropyridine-2-carbonyl)phenyl]propionate (1.52 g, 4.63 mmol) in dichloromethane (15 mL) and ethanol (15 mL) was added sodium borohydride (0.175 g, 4.63 mmol) under ice cooling, and the resulting solution was stirred at the same temperature for 1 hour. The reaction solution was concentrated under reduced pressure. The residue was dissolved in water and ethyl acetate. To the solution was added acetic acid and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium bicarbonate solution and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1), to thereby yield 0.264 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236826B2
Source datasetuspto-grants-2012_08
ORD IDord-38a51d03d22c401fb1bb0de4b1ee71d4
Source noteuspto-grants-2012_08