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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210158Generated: November 2, 2026

Sodium borohydride → 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propyloxy]pyridine

https://huagongshe.com/reaction/2210158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3-Phthalimidopropyloxy)pyridineHCID 19079090—
SolventEthanolHCID 702—
Product4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propyloxy]pyridineHCID 1907919854.2%

Reaction Steps

Sodium borohydride [1.89 g (50 mmol)] was added to a solution of 2.82 g (10.0 mmol) of 4-(3-phthalimidopropyloxy)pyridine in 150 ml of ethanol. The mixture was stirred at room temperature for 15 minutes. After the solvent was distilled off, brine was added to the residue. The mixture was extracted with chloroform and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10), and then recrystallized from ethyl acetate to obtain 1.54 g of the desired compound (yield: 54.2%, colorless crystals)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-589896f253964c8bb0a858c114933e6f
Source noteuspto-grants-1995_10