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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6158Generated: October 26, 2026

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

https://huagongshe.com/reaction/6158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1H-Isoindole-1,3(2H)-dione, 2-[3-(4-pyridinylthio)propyl]-HCID 19079118—
ReactantEthanol ethylacetateHCID 21584252—
SolventEthanolHCID 702—
Product4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propylthio)pyridineHCID 5712250554.4%

Reaction Steps

To a solution of 5.97 g (20.0 mmol) of 4-(3-phthalimidopropylthio)pyridine in 300 ml of ethanol, 1.51 g (40 mmol) of sodium borohydride was added, and the mixture was stirred at room temperature for 5 hours. The solvent was distilled off and saturated saline was added to the residue. The mixture was extracted with chloroform and the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethanol/ethyl acetate =1:10 to give 3.27 g of the desired compound (54.4% yield, colorless crystals), mp. 132°-134° C. NMR (200 MHz, CDCl3) δ: 2.11 (2H, m), 2.97 (2H, m), 3.72 (2H, m), 5.83 (1H, s), 6.98 (2H, d, J=5.4 Hz), 7.47-7.67 (3H, m), 7.77 (1H, dd, J=7.6, 1.2 Hz), 8.02 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-f61c39e9b64e46f3aa67a30fba7b886d
Source noteuspto-grants-1993_09