HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → 2'-Fluoro-5'-(2-oxoacetyl)biphenyl-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 5'-Acetyl-2'-fluorobiphenyl-2-carbonitrile | HCID 22273602 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'-Fluoro-5'-(2-oxoacetyl)biphenyl-2-carbonitrile | HCID 22273594 | — |
Reaction Steps
5′-Acetyl-2′-fluorobiphenyl-2-carbonitrile (0.31 g, 1.3 mmol) was suspended in 1,4-dioxane (4.75 ml) and water (0.25 ml) and warmed to 60° C. to solubilise the starting material. The solution was then cooled to ambient temperature, selenium dioxide (0.17 g, 1.55 mmol) added and the mixture heated under reflux for 2 h. The mixture was then allowed to cool to 60° C., activated charcoal (1 g) added and the mixture stirred for 30 min. The mixture was then allowed to cool to ambient temperature, filtered through a glass fibre filter paper and the solid washed with 1,4-dioxane (10 ml) and the filtrate evaporated to give crude 2′-fluoro-5′-(2-oxoacetyl)biphenyl-2-carbonitrile which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969716B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-6088685a4c1046deb56f1eebd6f7d5ef |
| Source note | uspto-grants-2005_11 |