HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926442Generated: October 25, 2026
Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate
https://huagongshe.com/reaction/926442
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
30 g of tricyclohexylbenzene was dissolved in 50 ml of methylene chloride, followed by cooling/stirring at 3° C., and 15.2 g of chlorosulfonic acid was slowly added dropwise. After the dropwise addition, the mixture was stirred at room temperature for 5 hours, charged with 10 g of ice, and further charged with 40 g of an aqueous 50% sodium hydroxide solution. Furthermore, 20 g of ethanol was added, followed by stirring at 50° C. for 1 hour, and after removing insoluble matters by filtration, the filtrate was distilled off under reduced pressure at 40° C. The precipitated crystal was collected by filtration and subjected to hexane washing 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 | US09285679B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-07db6bcd88354a1789b97d2ed4991738 |
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| Source note | uspto-grants-2016_03 |
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