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 stirred under cooling at 3° C. Thereto, 40.4 g of cyclohexyl chloride was slowly added dropwise. After the dropwise addition, the mixture 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 at 40° C. under reduced pressure, further distilled at 170° C. under reduced pressure, then cooled to room temperature, and recrystallized by charging 50 ml of acetone. 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 | US08999621B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-08137f861f4e4d6dae76c3d526fbcaa2 |
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| Source note | uspto-grants-2015_04 |
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