HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982158Generated: October 28, 2026
4-Bromopyridine → 8-Bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-ol
https://huagongshe.com/reaction/1982158
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromopyridine | HCID 14268 | — |
| Reactant | 8-bromodibenz[b,f]oxepin-10(11H)-one | HCID 12245878 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506752 | HCID 178506752 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 8-Bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-ol | HCID 13608612 | 26.2% |
Reaction Steps
Under an argon atmosphere, a solution of 4-bromopyridine (16.6 g) in anhydrous ether (90 ml) previously cooled to -40°, was transferred slowly via a cannular to a stirred solution of n-butyl lithium in hexane (1.55M; 68 ml) cooled to -78°. The mixture was stirred at -78° for 20 minutes and the resulting 4-lithiopyridine was transferred to a chilled (-78°) stirred suspension of 8-bromodibenz[b,f]oxepin-10(11H)-one (15 g) in anhydrous ether (100 ml). The reaction was stirred at -78° for 30 minutes, then the cooling bath was removed and the mixture was treated with 100 ml of water and allowed to warm to room temperature. The solids were filtered off, washed with water and dried to give 5.0 g of 8-bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-ol. The mother liquor was worked up and a total of 9.4 grams of the starting ketone 8-bromodibenz[b,f]oxepin-10(11H)-one were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595689 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-8537de479302484e9b21610f229c08e7 |
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| Source note | uspto-grants-1986_06 |
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