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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035325Generated: November 1, 2026

Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate

https://huagongshe.com/reaction/2035325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantChlorosulfonic acidHCID 24638—
ReactantTricyclohexylbenzeneHCID 3015433—
SolventDichloromethaneHCID 6344—
ProductSodium 1,3,5-tricyclohexylbenzenesulfonateHCID 86655172151.4%

Reaction Conditions

Temperature3 °C

Reaction Steps

Tricyclohexylbenzene (30 g) was dissolved in 50 ml of methylene chloride, followed by stirring under cooling at 3° C., and 15.2 g of chlorosulfonic acid was slowly added dropwise thereto. After the dropwise addition, the resultant was stirred at room temperature for 5 hours, and 10 g of ice was added thereto. Subsequently, 40 g of 50% aqueous sodium hydroxide solution was added thereto, and 20 g of ethanol was further added thereto. The resultant was stirred at 50° C. for an hour, the insoluble fraction was then removed by filtering, and the resultant was removed by distillation under reduced pressure at 40° C. The precipitated crystals were collected through filtering and washed with hexane, thereby obtaining 30 g of sodium 1,3,5-tricyclohexylbenzene sulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08574814B2
Source datasetuspto-grants-2013_11
ORD IDord-b800b823e37644b090d24a3e166623ea
Source noteuspto-grants-2013_11