Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Decalin | HCID 7044 | — |
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 9H-Tribenzo[b,d,f]azepine | HCID 11299519 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22501123 | HCID 22501123 | 25.1% |
Reaction Steps
A mixture of 9.2 g (38 mmol) of 9H-tribenz[b,d,f]azepine (synthesized in accordance with J. Org. Chem., vol. 56, p. 3906 (1991)), 44.8 g (190 mmol) of 1,4-dibromobenzene, 5.6 g (100 mmol) of potassium hydroxide, 1.6 g (25 mmol) of copper powder, and 50 ml of decalin was heated at an external temperature of 200° C. for 36 hours in a nitrogen stream while stirring. The reaction mixture was cooled nearly to room temperature, chloroform was added thereto, followed by filtration using Celite to remove the insoluble matter. The filtrate was concentrated. To remove decalin, n-hexane was added to the residue, followed by filtration. The filter cake was purified by silica gel column chromatography to give 3.8 g (25%) of 9-(4-bromophenyl)-9H-tribenz[b,d,f]azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413657B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-e3c9982081c44f9597bec9d3655c8635 |
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| Source note | uspto-grants-2002_07 |
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