Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorocyclohexane | HCID 10952 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Tricyclohexylbenzene | HCID 3015433 | 50.7% |
Reaction Steps
Aluminum chloride (6.83 g) was added to 20.0 g of benzene, and the mixture was cooled with stirring at 3° C. Thereto, 40.4 g of cyclohexyl chloride was gradually added dropwise. After the dropwise addition, the reaction solution was stirred at room temperature for 5 hours and then poured in ice water. The organic layer was extracted with ethyl acetate, and the obtained organic layer was distilled off under reduced pressure at 40° C. and further distilled off under reduced pressure at 170° C. The residue was cooled, to room temperature, and 50 ml of acetone was added thereto for recrystallization. The precipitated crystal was collected by filtration to obtain 14 g of tricyclohexylbenzene.
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-57c4044c53b149dca6e12b2b77b51d97 |
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| Source note | uspto-grants-2015_07 |
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