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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,6-Dibromonaphthalene | HCID 640591 | — |
| Reactant | Dibenzo(b,d)furan-2-ylboronic Acid (contains varying amounts of Anhydride) | HCID 12032376 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(6-Bromonaphthalen-2-yl)dibenzofuran | HCID 58569057 | 40.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940412B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-cc5c485afd43429288c31c60f9ca9747 |
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| Source note | uspto-grants-2015_01 |
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