HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloropyridine → 5-Chloro-2-(2-morpholinobenzoyl)-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloropyridine | HCID 12288 | — |
| Reactant | Ethyl 5-chlorobenzofuran-2-carboxylate | HCID 2799299 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-(2-morpholinobenzoyl)-benzofuran | HCID 69284462 | — |
Reaction Steps
A solution of ethyl 5-chlorobenzofuran-2-carboxylate (350 mg, 1.56 mmol) in THF (10 ml) is added at −70° C. to a THF solution of lithiated 4-chloropyridine (1.8 mmol prepared according to G. Quéguiner et al., Synthesis 1986, 886-891). The mixture is allowed to reach room temperature within 16 hours before quenching with acetic acid. The product is extracted with chloroform. Drying and chromatography on silicagel gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486996B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-87f9061cd16240e8b1cc4d37ba8988e8 |
| Source note | uspto-grants-2013_07 |