Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Bromo-3,5-dimethylpyridin-1-ium-1-olate | HCID 12493036 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-3,5-dimethylpyridine | HCID 22323246 | 38% |
Reaction Steps
To a microwave tube was added 4-bromo-3,5-dimethylpyridine 1-oxide (2.00 g, 9.90 mmol), triphenylphosphine (3.12 g, 11.9 mmol) and toluene (10 mL). The tube was sealed and heated at 180° C. overnight. The reaction solution was diluted with ethyl acetate, and filtered. The filtrate was concentrated and purified by flash chromatography (10% to 40% ethyl acetate in hexanes) to afford the desired product as a yellow oil (700 mg, 38%). 1H NMR (400 MHz, CDCl3): δ 8.22 (s, 2H), 2.38 (s, 6H); LCMS calculated for C2H9BrN(M+H)+: m/z=186.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563541B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-70b403db2f374c058d9b4b974006ecdc |
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| Source note | uspto-grants-2013_10 |
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