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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N,N-bis(2-chloroethyl)-p-toluenesulphonamide | HCID 96039 | — |
| Reactant | 4-Methoxy-3,5-dimethylaniline HCl | HCID 19032380 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazine | HCID 19032387 | 50.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650411 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-defd8b78b9dd4aa5ae0b400304ec643c |
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| Source note | uspto-grants-1997_07 |
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