HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-Cyclobutanecarbonylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Pyridine-2-carbonitrile | HCID 7522 | — |
| Reactant | HCID 178419648 | HCID 178419648 | — |
| Product | 2-Cyclobutanecarbonylpyridine | HCID 24723549 | 83% |
Reaction Steps
To an etheral solution of cyclobutyl magnesium bromide (prepared from bromocyclobutane (970 mg, 7.18 mmol) and magnesium (175 mg, 7.18 mmol) in ether (20 ml)) was dropwise added a solution of 2-cyanopyridine (748 mg, 7.18 mmol) in ether (10 ml) at room temperature. After 2 hours, the reaction was quenched by addition of an aqueous saturated solution of NH4Cl. The mixture was extracted with ether. The organic phase was dried over MgSO4 and concentrated under vacuum. The residue was purified by chromatography on silica gel (hexane/AcOEt 95/5) to give the cyclobutyl(2-pyridinyl)methanone 7 as colorless oil (960 mg, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361668B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-711f7bdcc41d46af90418bca0e9ffc6c |
| Source note | uspto-grants-2008_04 |