Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429337Generated: October 30, 2026

1,2-Dimethoxyethane → 2-(6-Bromonaphthalen-2-yl)dibenzofuran

https://huagongshe.com/reaction/1429337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant2,6-DibromonaphthaleneHCID 640591—
ReactantDibenzo(b,d)furan-2-ylboronic Acid (contains varying amounts of Anhydride)HCID 12032376—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2-(6-Bromonaphthalen-2-yl)dibenzofuranHCID 5856905740.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

In argon atmosphere, a mixture of 18.53 g (87.4 mmol) of 2-dibenzofuranboronic acid, 25.00 g (87.4 mmol) of 2,6-dibromonaphthalene, 5.05 g (4.40 mmol) of tetrakis(triphenylphosphine)palladium (0), 300 ml of dimethoxyethane, and 132 g of a 2 M sodium carbonate aqueous solution was stirred at a bath temperature of 85° C. for 7 h. The reaction mixture was added with water and extracted with toluene. After washing with water, the organic phase was dried over magnesium sulfate. Then, the solvent was removed by distillation under reduced pressure, and the residue was purified by silica gel chromatography to obtain 13.20 g (yield: 38%) of 2-(6-bromonaphthalene-2-yl)dibenzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940412B2
Source datasetuspto-grants-2015_01
ORD IDord-cc5c485afd43429288c31c60f9ca9747
Source noteuspto-grants-2015_01