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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromopyridineHCID 14268—
Reactant8-bromodibenz[b,f]oxepin-10(11H)-oneHCID 12245878—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178506752HCID 178506752—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product8-Bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-olHCID 1360861226.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595689
Source datasetuspto-grants-1986_06
ORD IDord-8537de479302484e9b21610f229c08e7
Source noteuspto-grants-1986_06