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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27729Generated: October 25, 2026

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

https://huagongshe.com/reaction/27729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactantp-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
SolventWaterHCID 962—
Product4-(4-(Methylsulfonyl)piperazin-1-yl)phenolHCID 640049—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04223036
Source datasetuspto-grants-1980_09
ORD IDord-6d78a14e4bea4668a79fff0ca30a4176
Source noteuspto-grants-1980_09