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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2198526생성일: 2026년 10월 25일

Ethanol → 4-(4-(Methylsulfonyl)piperazin-1-yl)phenol

https://huagongshe.com/reaction/2198526

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Sodium BicarbonateHCID 516892—
반응물p-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
용매WaterHCID 962—
생성물4-(4-(Methylsulfonyl)piperazin-1-yl)phenolHCID 640049—

반응 단계

To a stirred mixture of 12.9 parts of 4-(1-piperazinyl)-phenol dihydrobromide, 40 parts of ethanol and 50 parts of water are added 12.6 parts of sodium hydrogen carbonate. Then there are added dropwise 6.4 parts of methanesulfonyl chloride at 0° C. Upon completion, stirring is continued overnight. The precipitated product is filtered off and taken up in water. The whole is alkalized with a sodium hydroxide solution and stirred for 30 minutes at room temperature. The mixture is filtered over hyflo and the filtrate is acidified with acetic acid. The precipitated product is filtered off and dried, yielding 2.8 parts of 1-(4-hydroxyphenyl)-4-(methylsulfonyl)-piperazine; mp. 204.9° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04358449
출처 데이터셋uspto-grants-1982_11
ORD IDord-ec80264623f1485e9509d3d39ae6ff60
출처 메모uspto-grants-1982_11