HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 2-Ethynyl-5-methylpyridine | HCID 13400634 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine | HCID 86729575 | — |
Reaction Steps
To the solution of 2-ethynyl-5-methylpyridine (12-2) (1.38 g, 11.8 mmol) in tert-butyl alcohol (4.734 g, 63.9 mmol) was added potassium tert-butoxide (531 mg, 4.7 mmol) under nitrogen. The solution was heated to reflux for overnight. The solvent was removed under reduced pressure. The residue was purified by silca gel chromatography with the gradient eluent (PE/EA/NEt3=10/1/1%; 5/1/1%). The product (Z)-2-(2-tert-butoxyvinyl)-5-methylpyridine (12-3) was obtained as yellow oil (1.40 g, 62%) and by product was (E)-2-(2-tert-butoxyvinyl)-5-methylpyridine (0.3 g, 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062059B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-49e0f60196d24fdfae3616ed280245d7 |
| Source note | uspto-grants-2015_06 |