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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274731Generated: November 2, 2026

Triethylamine → 4-(4-Chlorobutylthio)pyridine

https://huagongshe.com/reaction/274731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
Reactantpyridine-4-thiolHCID 178418431—
SolventEthanolHCID 702—
Product4-(4-Chlorobutylthio)pyridineHCID 1581697889.7%

Reaction Steps

To a suspension of 33.35 g (0.30 mol) of 4mercaptopyridine and 51.44 g (0.30 mol) of 1-bromo-4-chlorobutane in 500 ml of ethanol, 41.9 ml (0.30 mol) of triethylamine was added, and the mixture was stirred at room temperature for 5 hours. The solvent was distilled off and chloroform was added to the residue. The mixture was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate/n-hexane=1:1) to give 54.27 g of the desired compound (89.7% yield, colorless oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-a2ab11f6bfd540a7ac19a0758a813ac0
Source noteuspto-grants-1995_02