HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 2-Phenylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2-(2,4-Difluorophenyl)-4-chloropyridine | HCID 68645902 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenylpyridine | HCID 13887 | 126% |
Reaction Steps
44.9 mg (0.2 mmol) of palladium acetate, 70 mg (0.2 mmol) of 2-(dicyclohexylphosphino)biphenyl, 1.3455 grams (14 mmol) of sodium t-butoxide, 1.1281 grams (5 mmol) of 2-(2,4-difluorophenyl)-4-chloropyridine, and 0.7029 grams (6 mmol) of indole were mixed with 60 ml of toluene and refluxed for 48 hours. Next a double portion of the catalyst package and one more portion of indole was added to the mixture to reflux for 72 hours. The reaction contents were cooled to room temperature, diluted with dichloromethane and preabsorbed onto silica and chromatographed using methylene chloride eluent to isolate 0.978 grams of yellow solid in 63% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816016B1 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-23c56ae5a265462d94daf1039cd93230 |
| Source note | uspto-grants-2010_10 |