Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | HCID 86682766 | HCID 86682766 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 86682765 | HCID 86682765 | — |
Reaction Steps
6-(fluoranthene-3-yl)naphthalene trifluoromethane sulfonate (0.16 g, 0.33 mmol), boronic acid (0.054 g, 0.36 mmol) and Pd(PPh3)4 (0.194 g, 0.17 mmol) were placed in a 2-neck RB flask and placed under nitrogen atmosphere. Toluene (25 mL) and Dimethoxyethane (25 mL) was then added to the reaction mixture followed by aq. Na2CO3 (2 M, 1.0 ml). The reaction mixture was refluxed at 85° C. for 24 h and diluted with Toluene and filtered through a celite bed. The combined organic extracts was evaporated to dryness and purified by silica column chromatography using dichloromethane and pet-ether (40-60° C.) to give slightly yellow coloured powder the product (0.05 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09410080B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-613f1ed54dfa489db044e462505bbb36 |
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| Source note | uspto-grants-2016_08 |
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