HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027349Generated: October 25, 2026
Ethanol → Sodium 1,3,5-tricyclohexylbenzenesulfonate
https://huagongshe.com/reaction/1027349
Participants
| Role | Name | HCID | Charge |
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| 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, and the solution was stirred under cooling at 3° C. Thereto, 15.2 g of chlorosulfonic acid was slowly added dropwise and after the dropwise addition, the reaction solution was stirred at room temperature for 5 hours. Subsequently, 10 g of ice was charged, and 40 g of an aqueous 50% sodium hydroxide solution was charged. Furthermore, 20 g of ethanol was added, and the mixture was stirred at 50° C. for 1 hour. Insoluble matters were removed by filtration, and the residue was distilled off under reduced pressure at 40° C. The precipitated crystals were collected by filtration and then 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 | US08735048B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-1ea40928f6ff43d2adaaf72d4e29f615 |
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| Source note | uspto-grants-2014_05 |
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