Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590895Generated: October 25, 2026

Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate

https://huagongshe.com/reaction/590895

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 amounting to 30 g was dissolved in 50 ml of methylene chloride and agitated while cooling at 3° C. Then, 15.2 g of chlorosulfonic acid was slowly dropped into the solution. After the completion of the dropping, the mixture was agitated at room temperature for five hours. Subsequently, 10 g of ice and then 40 g of 50% aqueous sodium hydroxide solution was poured into the mixture. Further, 20 g of ethanol was added and agitated at 50° C. for an hour. Any insoluble matter was removed by filtration, and the product was subjected to vacuum distillation at 40° C. The thus obtained crystal was collected by filtration, and washed with hexane, thereby obtaining 30 g of sodium 1,3,5-tricyclohexylbenzenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09235116B2
Source datasetuspto-grants-2016_01
ORD IDord-43f04fccdfa146fda9f1cee1f1fec542
Source noteuspto-grants-2016_01