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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266065Generated: October 26, 2026

Potassium Iodide → 4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazine

https://huagongshe.com/reaction/266065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCyclohexanolHCID 7966—
ReactantSodium CarbonateHCID 10340—
ReactantN,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
Reactant4-Methoxy-3,5-dimethylaniline HClHCID 19032380—
SolventWaterHCID 962—
Product4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazineHCID 1903238750.4%

Reaction Steps

A mixture of 10 g of 4-methoxy-3,5-dimethylbenzenamine hydrochloride, 19.9 g of N,N-bis(2-chloroethyl)-4-methylbenzenesulfonamide, 16.8 g of sodium carbonate, 0.5 g of potassium iodide and 100 ml of cyclohexanol was stirred overnight at 150°-160° C. After cooling, the reaction mixture was poured into water. The product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 1-butanol, yielding 10 g (50.4%) of 4-(4-methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazine; mp. 174.2° C. (interm. 42).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650411
Source datasetuspto-grants-1997_07
ORD IDord-defd8b78b9dd4aa5ae0b400304ec643c
Source noteuspto-grants-1997_07