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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210160Generated: October 30, 2026

Sodium borohydride → 4-(2-(2-Hydroxymethylbenzoyl)aminoethylthio]pyridine

https://huagongshe.com/reaction/2210160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Phthalimidoethylthio)pyridineHCID 19079256—
SolventEthanolHCID 702—
Product4-(2-(2-Hydroxymethylbenzoyl)aminoethylthio]pyridineHCID 1907917977.8%

Reaction Steps

To a solution of 2.84 g (10.0 mmol) of 4-(2-phthalimidoethylthio)pyridine in 150 ml of ethanol, 3.78 g (100 mmol) of sodium borohydride was added, and the mixture was stirred at room temperature for 3 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 2.24 g of the desired compound (77.8% yield, colorless crystals), mp. 132°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-dfa9350426e944b589ba9e4f5e0b284c
Source noteuspto-grants-1995_10