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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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물CyclohexanolHCID 7966—
반응물Sodium CarbonateHCID 10340—
반응물N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 96039—
반응물4-Methoxy-3,5-dimethylaniline HClHCID 19032380—
용매WaterHCID 962—
생성물4-(4-Methoxy-3,5-dimethylphenyl)-1-[(4-methylphenyl)sulfonyl]piperazineHCID 1903238750.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650411
출처 데이터셋uspto-grants-1997_07
ORD IDord-defd8b78b9dd4aa5ae0b400304ec643c
출처 메모uspto-grants-1997_07