HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429339Generated: October 31, 2026
Toluene → 2-(7-bromonaphthalene-2-yl)-9,9-dimethyl-9H-fluorene
https://huagongshe.com/reaction/1429339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,7-Dibromonaphthalene | HCID 625355 | — |
| Reactant | (9,9-Dimethyl-9H-fluoren-2-yl)boronic acid | HCID 22348454 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(7-bromonaphthalene-2-yl)-9,9-dimethyl-9H-fluorene | HCID 58569501 | 48% |
Reaction Steps
In argon atmosphere, a mixture of 16.65 g (69.9 mmol) of 9,9-dimethyl-9H-fluorene-2-ylboronic acid, 20.00 g (69.9 mmol) of 2,7-dibromonaphthalene, 4.04 g (3.50 mmol) of tetrakis(triphenylphosphine)palladium (0), 200 ml of toluene, 200 ml of dimethoxyethane, and 106 g of a 2 M sodium carbonate aqueous solution was stirred at 85° C. for 9 h and left standing overnight. The reaction mixture was added with water and stirred at room temperature for one hour. After filtration, the filtrate was extracted with toluene. The organic phase was washed with water and then with a saturated saline solution and dried over sodium sulfate, and then the toluene was removed by distillation under reduced pressure. The obtained brown oily substance was purified by silica gel chromatography to obtain 13.4 g (yield: 48%) of 2-(7-bromonaphthalene-2-yl)-9,9-dimethyl-9H-fluorene.
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-d82fd4f22f074e2ea132c149808685c0 |
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| Source note | uspto-grants-2015_01 |
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