HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429328Generated: October 30, 2026
1,2-Dimethoxyethane → 7-Bromo-2-(9-phenanthrenyl)naphthalene
https://huagongshe.com/reaction/1429328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,7-Dibromonaphthalene | HCID 625355 | — |
| Reactant | 9-Phenanthracenylboronic acid | HCID 11775704 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Bromo-2-(9-phenanthrenyl)naphthalene | HCID 57540015 | 38.7% |
Reaction Steps
In argon atmosphere, a mixture of 18.64 g (83.9 mmol) of 9-phenanthreneboronic acid, 30.00 g (104.9 mmol) of 2,7-dibromonaphthalene, 4.85 g (4.2 mmol) of tetrakis(triphenylphosphine)palladium (0), 200 ml of dimethoxyethane, 200 ml of toluene, and 106 ml of a 2 M sodium carbonate 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 toluene was removed by distillation under reduced pressure, and the residue was purified by silica gel chromatography to obtain 12.46 g (yield: 31.0%) of 7-bromo-2-(9-phenanthrenyl)naphthalene.
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-036d58eace664723946406ef9fdfad22 |
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| Source note | uspto-grants-2015_01 |
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