Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605955Generated: October 30, 2026

Potassium Iodide → 4'-{[2-[4-(p-fluorophenyl)-3,6-dihydro-1(2H)-pyridyl]-ethyl]thio}acetanilide

https://huagongshe.com/reaction/1605955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorophenyl)-1,2,3,6-tetrahydropyridineHCID 197748—
Reactant4'-[(2-Chloroethyl)thio]acetanilideHCID 19700369—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4'-{[2-[4-(p-fluorophenyl)-3,6-dihydro-1(2H)-pyridyl]-ethyl]thio}acetanilideHCID 21545621—

Reaction Steps

1.8 G. of 4'-[(2-chloroethyl)thio]acetanilide, 2.7 g. of 4-(p-fluorophenyl)-1,2,3,6-tetrahydropyridine, 4.5 g. of potassium carbonate and a few crystals of potassium iodide are heated under reflux conditions in 50 ml. of ethanol and 5 ml. of water for 16 hours. The solvent is evaporated under reduced pressure, the residue is taken up in chloroform and washed with water. From the organic phase there is obtained crude 4'-{[2-[4-(p-fluorophenyl)-3,6-dihydro-1(2H)-pyridyl]-ethyl]thio}acetanilide which melts at 150°-152°C. after recrystallization from acetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03951987
Source datasetuspto-grants-1976_04
ORD IDord-feec41f8f5934a3d9e43a861cc7ed94f
Source noteuspto-grants-1976_04