Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 3-Bromo-2-chloro-5-nitropyridine | HCID 230889 | — |
| Catalyst | 3375-31-3 | HCID 58759193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Nitrobenzofuro[2,3-b]pyridine | HCID 68619065 | 52.2% |
Reaction Steps
Potassium carbonate (87 mg) and phenol (47 mg) were added to an N,N-dimethylacetamide (1 ml) solution containing 3-bromo-2-chloro-5-nitropyridine (100 mg), followed by stirring at 70° C. for 3 hours. Acetic acid palladium (20 mg) was added in a nitrogen atmosphere, followed by stirring at 100° C. for 3.5 hours. Water was added, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, hexane and ethyl acetate were added to the obtained residue, an insoluble precipitate was collected by filtration, and a light yellow solid of 3-nitrobenzofuro[2,3-b]pyridine (47.1 mg) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809371B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-50655dca60054437842f1787d66784bb |
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| Source note | uspto-grants-2014_08 |
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