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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164254Generated: October 31, 2026

Ethanol → HCID 2399073, compound

https://huagongshe.com/reaction/2164254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium BicarbonateHCID 516892—
Reactantp-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
SolventWaterHCID 962—
ProductHCID 2399073HCID 2399073—

Reaction Steps

To a stirred mixture of 15.5 parts of 4-(1-piperazinyl)phenol dihydrobromide, 40 parts of ethanol and 75 parts of water are added 15.2 parts of 4-methylbenzenesulfonyl chloride and stirring is continued for 30 minutes at room temperature. Then there are added portionwise 12.6 parts of sodium hydrogen carbonate at 0° C. Upon completion, stirring is continued overnight at room temperature. The precipitated product is filtered off and taken up in alkaline water. The mixture is filtered over hyflo and the filtrate is acidified with acetic acid. The precipitated product is filtered off and taken up in water. The free base is liberated in the conventional manner with a sodium hydroxide solution. The whole is filtered over hyflo and the filtrate is acidified with acetic acid. The precipitated product is filtered off and dried, yielding 4.8 parts of 1-(4-hydroxyphenyl)-4-(4-methylphenylsulfonyl)piperazine; mp. 193.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04503055
Source datasetuspto-grants-1985_03
ORD IDord-897bb2741ecd4fe5975ef176a9d465c6
Source noteuspto-grants-1985_03