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 (6.38 g) was added to 20.0 g of benzene, followed by stirring under cooling at 3° C., and 40.4 g of cyclohexyl chloride was slowly added dropwise thereto. After the dropwise addition, the resultant was stirred at room temperature for 5 hours, and the obtained reaction solution was added to ice water. The organic layer was extracted by using ethyl acetate, and the obtained organic layer was removed by distillation at 40° C. under reduced pressure. The resultant was further removed by distillation at 170° C. under reduced pressure and then cooled to room temperature, and 50 ml of acetone was added thereto to cause recrystallization. The precipitated crystals were collected through filtering, thereby obtaining 14 g of tricyclohexylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574814B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-21951efda33b4875984a232e3799e524 |
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| Source note | uspto-grants-2013_11 |
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