HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(6-Chloropyridin-2-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 6-Chloropyridine-2-carbonitrile | HCID 118424 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(6-Chloropyridin-2-yl)ethanone | HCID 11579167 | — |
Reaction Steps
A solution of 2-chloro-6-cyanopyridine (50 g) in THF (400 ml) is cooled to −5° C. and a solution of methylmagnesium iodide in diethyl ether (3 M, 200 ml) is added. After 1 h at 0° C. the ether is destilled off and the THF-mixture is heated to 60° C. for 1 h. The THF is evaporated and the residue is treated with ice water and acidified with 2 M hydrochloric acid. The water phase is extracted with dichloromethane and after drying and evaporation of the organic phase, the residue is purified by silica-gel flash chromatography. The title compound is obtained as an oil (11.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528456B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-e9a636cca3c340d69cd851d12531c500 |
| Source note | uspto-grants-2003_03 |