HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Aminophenoxy)benzene → HCID 86617156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Aminophenoxy)benzene | HCID 8764 | — |
| Reactant | 2,4,6-Triphenylpyrylium tetrafluoroborate | HCID 9930615 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86617156 | HCID 86617156 | 95.8% |
Reaction Steps
A 1 L round-bottom flask equipped with a condenser was charged with 2,4,6-triphenyl-pyrylium tetrafluoroborate (50.0 g, 0.126 mole), 4-phenoxyaniline (25.7 g, 0.138 mole) and ethanol (400 mL). The resulting solution was magnetically stirred and refluxed under nitrogen atmosphere for 6 hours. The solution was cooled to room temperature, the condensation product precipitate out as cream color crystal. The crystal was collected by filtration and dried in vacuum oven (100° C.) to give the desired product (68 g, 95% yield). Mp=201.7 C
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928155B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-ed587a82427242f8940e6ea166a2b0d2 |
| Source note | uspto-grants-2011_04 |