HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Acetyl-5-bromopyridine | HCID 820423 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone | HCID 68670605 | 3,170.7% |
Reaction Steps
A stirred solution of 1-(5-bromopyridin-3-yl)ethanone (600 mg, 3.0 mmol), potassium isopopenyltrifluoroborate (148 mg, 3.0 mmol), and Et3N (1.25 mL, 9.0 mmol) in iPrOH (20 mL) and H2O (10 mL) was degassed with argon for 10 min and then PdCl2 (dppf).CH2Cl2 (74 mg, 0.09 mmol) was added and the reaction mixture was heated to reflux for 5 h. The solution was cooled to room temperature and diluted with Ether and H2O. The layers were separated and the aqueous layer was extracted with Ether (2×50 mL). The combined organic layer was washed with brine, dried with Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (30% EtOAc in hexanes) to provide 460 mg of 1-(5-(prop-1-en-2-yl)pyridin-3-yl)ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299267B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-0328a30d6b6c44d598c9f8922879ffcd |
| Source note | uspto-grants-2012_10 |