HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035325Generated: November 1, 2026
Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate
https://huagongshe.com/reaction/2035325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Tricyclohexylbenzene | HCID 3015433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Sodium 1,3,5-tricyclohexylbenzenesulfonate | HCID 86655172 | 151.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574814B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-b800b823e37644b090d24a3e166623ea |
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| Source note | uspto-grants-2013_11 |
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