Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Hexafluorobenzene | HCID 9805 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1,4-Bis(1-naphthoxy)tetrafluorobenzene | HCID 19879615 | — |
Reaction Steps
The monomer 1,4-bis(1-naphthoxy)tetrafluorobenzene (4FNE) was prepared as follows. A 100 mL round bottom flask equipped with a magnetic stirrer was charged with hexafluorobenzene (3.53 g, 0.0190 mole), 1-naphthol, and DMAc (50 mL). After the solids dissolved, potassium carbonate (6.50 g, 0.048 mole) was added and the mixture was heated at about 140° C. for 2 hr. The mixture was then cooled to room temperature, filtered, and poured into toluene (150 mL). The toluene solution was washed twice with water (2×150 mL) and concentrated by rotary evaporation to yield an off-white powder (7.91 g). Analysis of the powder by GC showed a mixture of isomers (2% ortho, 8% meta, and 90% para). The powder was recrystallized from a mixture of N,N-dimethylformamide (DMF) and water to yield the desired all-para 4FNE, GC/MS (m+ /e 434).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05108840 |
|---|
| Source dataset | uspto-grants-1992_04 |
|---|
| ORD ID | ord-e6d43dddf9544c719bdb39274ca9741e |
|---|
| Source note | uspto-grants-1992_04 |
|---|