Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylsilane | HCID 70435 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Product | HCID 63656854 | HCID 63656854 | 5% |
Reaction Steps
4-bromobut-1-ynyl)trimethylsilane (700 mg, 3 mmol), pyridin-2-ol (300 mg, 3 mmol) and K2CO3 (900 mg, 6 mmol) were poured into acetone (4.2 ml) and the resulting mixture was heated in the microwave at 150° C. for 7 min. The solvent was evaporated and the crude product was dissolved DCM and the organic layer was washed with water. The crude residue was purified over silicagel chromatography (prepacked 5 g silicagel column, DCM/MeOH: 99/1 as eluent) to afford 33 mg of 1-(but-3-ynyl)pyridin-2(1H)-one as a brown oil (Yield: 5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08883826B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7b0668091d8a41daa1dcc5e7ddc24042 |
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| Source note | uspto-grants-2014_11 |
|---|