Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6156Generated: October 29, 2026

Sodium borohydride → 4-[3-(2-Hydroxymethylbenzoyl)aminopropylthio]pyridine

https://huagongshe.com/reaction/6156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1H-Isoindole-1,3(2H)-dione, 2-[3-(4-pyridinylthio)propyl]-HCID 19079118—
SolventEthanolHCID 702—
Product4-[3-(2-Hydroxymethylbenzoyl)aminopropylthio]pyridineHCID 1907914278.2%

Reaction Steps

To a solution of 5.97 g (20.0 mmol) of 4-(3-phthalimidopropylthio)pyridine in 300 ml of ethanol, 7.57 g (200 mmol) of sodium borohydride was added, and stirred at room temperature for 24 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 4.73 g of the desired compound (78.2% yield, colorless crystals), mp. 110°-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-f7c946d278a44fe28f799ef9783e5d4b
Source noteuspto-grants-1993_09