Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Hexafluoropropylene oxide | HCID 9883 | — |
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Hydrofluoric Acid | HCID 14917 | — |
| Product | bisphenol AF | HCID 73864 | 86.4% |
Reaction Steps
A mixture of 228 g of hexafluoropropene epoxide and 72 g of hexafluoropropene, and also 220 g of hydrogen fluoride were filled into a 1 liter capacity stainless steel autoclave without a stirring device and the mixture was heated for 20 hours at 100° C. The reaction product, which consisted of a solution of hexafluoroacetone in hydrogen fluoride, was transferred by exploiting its own vapor pressure to a 2.7 liter capacity nickel autoclave, which already contained 258 g of phenol, and the resulting mixture was heated for 8 hours at 100° C. After the hydrogen fluoride and the hexafluoropropene, which did not take part in the reaction, had been distilled off, 399 g of hexafluoro-2,2-bis-(4-hydroxyphenyl)-propane were obtained. This corresponds to a yield of 86.4% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04400546 |
|---|
| Source dataset | uspto-grants-1983_08 |
|---|
| ORD ID | ord-87c9c8af31224fa5a1a3271faeae1f15 |
|---|
| Source note | uspto-grants-1983_08 |
|---|