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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926442Generated: October 25, 2026

Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate

https://huagongshe.com/reaction/926442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantChlorosulfonic acidHCID 24638—
ReactantTricyclohexylbenzeneHCID 3015433—
SolventDichloromethaneHCID 6344—
ProductSodium 1,3,5-tricyclohexylbenzenesulfonateHCID 86655172—

Reaction Conditions

Temperature3 °C

Reaction Steps

30 g of tricyclohexylbenzene was dissolved in 50 ml of methylene chloride, followed by cooling/stirring at 3° C., and 15.2 g of chlorosulfonic acid was slowly added dropwise. After the dropwise addition, the mixture was stirred at room temperature for 5 hours, charged with 10 g of ice, and further charged with 40 g of an aqueous 50% sodium hydroxide solution. Furthermore, 20 g of ethanol was added, followed by stirring at 50° C. for 1 hour, and after removing insoluble matters by filtration, the filtrate was distilled off under reduced pressure at 40° C. The precipitated crystal was collected by filtration and subjected to hexane washing to obtain 30 g of sodium 1,3,5-tricyclohexylbenzenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09285679B2
Source datasetuspto-grants-2016_03
ORD IDord-07db6bcd88354a1789b97d2ed4991738
Source noteuspto-grants-2016_03