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HRID 27729作成日:2026年10月25日

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

https://huagongshe.com/reaction/27729

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Sodium BicarbonateHCID 516892—
反応物p-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
溶媒WaterHCID 962—
生成物4-(4-(Methylsulfonyl)piperazin-1-yl)phenolHCID 640049—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04223036
出典データセットuspto-grants-1980_09
ORD IDord-6d78a14e4bea4668a79fff0ca30a4176
出典メモuspto-grants-1980_09