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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6165Generated: October 29, 2026

Benzoyl chloride → 4-[4-(Benzoylamino)butylthio]pyridine

https://huagongshe.com/reaction/6165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-[(Pyridin-4-yl)sulfanyl]butan-1-amineHCID 13557537—
SolventDichloromethaneHCID 6344—
Product4-[4-(Benzoylamino)butylthio]pyridineHCID 1907917034.4%

Reaction Steps

To a solution of 1.00 g (5.49 mmol) of 4-(4-aminobutylthio)pyridine and 0.92 ml (6.60 mmol) of triethylamine in 30 ml of methylene chloride, 0.67 ml (5.77 mmol) of benzoyl chloride was added with stirring under ice-cooling and the mixture was stirred at room temperature for 13 hours. The mixture was washed with saturated aqueous sodium bicarbonate and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate) to give 0.54 g of the desired compound (34.4% yield, colorless crystals), mp. 75°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-b219b6ddb6814fc39f98caa37e23e5ac
Source noteuspto-grants-1993_09