Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(5-bromopyridin-2-yl)benzaldehyde | HCID 11849714 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11849758 | HCID 11849758 | 79% |
Reaction Steps
To a stirred solution of 6 (10 mmol) in 40 mL dry 1,4-dioxane was added palladium tetrakis-triphenylphosphine (400 mg), then 5-(diethoxymethyl-furan-2-yl)-trimethylstannane (10 mmol) was added and the reaction mixture was refluxed at 100° C. for 24 h. The solvent was then evaporated to dryness to give a dark brown residue that was suspended in water and extracted with CH2Cl2. The organic layer was passed over hyflo, dried (Na2SO4) and evaporated to dryness under reduced pressure, followed by acid hydrolysis with 2M HCl to furnish 7. Yield 79%; mp 204-206° C. (EtOH). 1H NMR (DMSO-d6); δ 7.55 (d, J=3.6 Hz, 1H), 7.73 (d, J=3.6 Hz, 1H), 8.06 (d, J=8.4 Hz, 2H), 8.27 (d, J=8.4 Hz, 1H), 8.37-8.41 (m, 3H), 9.24 (d, J=2.1 Hz, 1H), 9.67 (s, 1H), 10.09 (s, 1H). 13C NMR (DMSO-d6); δ 192.8, 178.1, 155.2, 154.7, 152.3, 146.3, 142.9, 136.5, 133.3, 130.0, 127.2, 125.1, 124.3, 121.4, 110.6. Anal. Calc. for C17H11NO3: C %, 73.63; H %, 3.99. Found C %, 73.75; H %, 3.81.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188121B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-dd16e7afd188470e83b10793dfb60169 |
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| Source note | uspto-grants-2012_05 |
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