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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530157Generated: October 26, 2026

Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate

https://huagongshe.com/reaction/1530157

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

Tricyclohexylbenzene (30 g) was dissolved in 50 ml of methylene chloride, and the resulting solution was cooled with stirring at 3° C. Thereto, 15.2 g of chlorosulfonic acid was gradually added dropwise. After the dropwise addition, the reaction solution was stirred at room temperature for 5 hours, and 10 g of ice was poured thereinto. Furthermore, 40 g of an aqueous 50 mass % sodium hydroxide solution was poured therein, and 20 g of ethanol was then added. This mixture was stirred at 50° C. for 1 hour, and insoluble matters were removed by filtration. The residue was distilled off under reduced pressure at 40° C., and the precipitated crystal was collected by filtration and washed with hexane to obtain 30 g of sodium 1,3,5-tricyclohexylbenzenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090722B2
Source datasetuspto-grants-2015_07
ORD IDord-8fcf397e0bc84d07ae738993af245900
Source noteuspto-grants-2015_07