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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044405Generated: October 26, 2026

Potassium Carbonate → 4-(4-chlorobenzylthio)pyridin-2(1H)-one

https://huagongshe.com/reaction/1044405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobenzyl mercaptanHCID 80409—
Reactant4-Chloropyridin-2-olHCID 2757611—
SolventDichloromethaneHCID 6344—
Product4-(4-chlorobenzylthio)pyridin-2(1H)-oneHCID 58580248—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloropyridin-2(1H)-one (100 mg, 0.77 mmol), K2CO3 (320 mg, 2.32 mmol) and (4-chlorophenyl)methanethiol (612 mg, 3.86 mmol) was stirred at 100° C. for 18 hours. After cooling the reaction to RT and was dilution with CH2Cl2 (5 mL), the crude product was subjected to flash chromatography (silica gel/hexane-EtOAc 100:0 to 0:100 gradient, employing LC-MS to identify the fractions containing the desired product) to afford 4-(4-chlorobenzylthio)pyridin-2(1H)-one 8A (96 mg, 46.9% yield). 1H NMR (400 MHz, Chloroform-D) δ ppm 12.30 (1H, br. s.), 7.28-7.43 (4H, m), 7.15 (1H, d, J=7.03 Hz), 6.28 (1H, d, J=1.51 Hz), 6.11 (1H, dd, J=6.90, 1.88 Hz), 4.11 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563583B2
Source datasetuspto-grants-2013_10
ORD IDord-eaece1f5915746189f97693d48383c3f
Source noteuspto-grants-2013_10