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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210164Generated: October 29, 2026

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

https://huagongshe.com/reaction/2210164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14538888HCID 14538888—
SolventEthanolHCID 702—
Product4-[4-(3-Hydroxyisoindolin-1-on-2-yl)butylthio]pyridineHCID 1907907627.5%

Reaction Steps

To a solution of 6.25 g (20.0 mmol) of 4-(4-phthalimidobutylthio)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 2.5 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: ethyl acetate) to give 1.73 g of the desired compound (27.5% yield, colorless crystals), mp. 144°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-2dd1e8a16d0348159777cb805c2d5edd
Source noteuspto-grants-1995_10