HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530157Generated: October 26, 2026
Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate
https://huagongshe.com/reaction/1530157
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 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090722B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-8fcf397e0bc84d07ae738993af245900 |
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| Source note | uspto-grants-2015_07 |
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