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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198526Generated: October 25, 2026

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

https://huagongshe.com/reaction/2198526

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 numberUS04358449
Source datasetuspto-grants-1982_11
ORD IDord-ec80264623f1485e9509d3d39ae6ff60
Source noteuspto-grants-1982_11