HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 1,2,4,6-Tetraphenylpyridin-1-ium tetrafluoroborate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2,4,6-Triphenylpyrylium tetrafluoroborate | HCID 9930615 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,2,4,6-Tetraphenylpyridin-1-ium tetrafluoroborate | HCID 12665546 | 87% |
Reaction Steps
A 500 mL round-bottomed flask equipped with a condenser was charged with 2,4,6-triphenyl-pyrylium tetrafluoroborate (22.4 g, 0.056 mole), aniline (5.8 g, 0.060 mole) and ethanol (200 mL). The resulting solution was magnetically stirred and refluxed under a nitrogen atmosphere for 6 hours. The solution was cooled to room temperature, and the product 27 precipitated as greenish-yellow, crystalline solid. The product was collected by filtration and dried in a vacuum oven at 100° C. (23 g, 87% yield). Mp=253° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915332B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-682788a548194c61998a1337d51cc3c6 |
| Source note | uspto-grants-2011_03 |