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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964162Generated: October 30, 2026

Triethylamine → 4-(4-Chlorobutylthio)pyridine

https://huagongshe.com/reaction/964162

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 4-mercaptopyridine 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 numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-7f05c3424a50446c8f2615d14a3b2f3b
Source noteuspto-grants-1998_06