HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815611Generated: October 26, 2026
1,4-Dibromobenzene → HCID 22501123, compound
https://huagongshe.com/reaction/1815611
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | Decalin | HCID 7044 | — |
| 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 worked up in the same manner as in Example 1, and the resulting crude product 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 | US06878822B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-eafe35d27d1c4099b5840f1d79cf0168 |
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| Source note | uspto-grants-2005_04 |
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