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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027349Generated: October 25, 2026

Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate

https://huagongshe.com/reaction/1027349

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, and the solution was stirred under cooling at 3° C. Thereto, 15.2 g of chlorosulfonic acid was slowly added dropwise and after the dropwise addition, the reaction solution was stirred at room temperature for 5 hours. Subsequently, 10 g of ice was charged, and 40 g of an aqueous 50% sodium hydroxide solution was charged. Furthermore, 20 g of ethanol was added, and the mixture was stirred at 50° C. for 1 hour. Insoluble matters were removed by filtration, and the residue was distilled off under reduced pressure at 40° C. The precipitated crystals were collected by filtration and then washed with hexane to obtain 30 g of sodium 1,3,5-tricyclohexylbenzenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735048B2
Source datasetuspto-grants-2014_05
ORD IDord-1ea40928f6ff43d2adaaf72d4e29f615
Source noteuspto-grants-2014_05