Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266065생성일: 2026년 10월 26일
Potassium Iodide → 4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazine
https://huagongshe.com/reaction/266065
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Cyclohexanol | HCID 7966 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | N,N-bis(2-chloroethyl)-p-toluenesulphonamide | HCID 96039 | — |
| 반응물 | 4-Methoxy-3,5-dimethylaniline HCl | HCID 19032380 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazine | HCID 19032387 | 50.4% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05650411 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-defd8b78b9dd4aa5ae0b400304ec643c |
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| 출처 메모 | uspto-grants-1997_07 |
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