Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Ethenyl-5-nitropyridine | HCID 23090550 | 111.6% |
Reaction Steps
0.5 g of 2-chloro-5-nitro-pyridine (3.15 mmol), 1.2 g of tributyl-vinyl-stannane (3.78 mmol), 0.036 g of tetrakistriphenylphosphinpalladium(0) (0.03 mmol), and 0.024 g of triphenylphosphin (0.09 mmol) were dissolved in 20 ml of toluene and stirred for 2 h under reflux. Upon cooling to room temperature, 10 ml of water were added, the aqueous layer was extracted with ethyl acetate, and the combined organic layers were washed with saturated sodium chloride, dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure. The crude product was purified via silica gel chromatography with cyclohexane/ethyl acetate (10%). Fractions containing the product were combined, the solvent evaporated to yield 0.528 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851463B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-b7e49e1d7a8c4bd78b33062ea0e82178 |
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| Source note | uspto-grants-2010_12 |
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