HuagongsheHuagongshe Chemistry Print Report · For research reference only
bisphenol AF → 4-[1,1,1,3,3,3-Hexafluoro-2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | bisphenol AF | HCID 73864 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178503044 | HCID 178503044 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-[1,1,1,3,3,3-Hexafluoro-2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol | HCID 2782224 | 56% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
Into a stainless steel autoclave were placed 500 g of 4,4'-(perfluoroisopropylidene)diphenol, 100 ml of isopropanol and 2 g of 5% ruthenium-carbon. The mixture was maintained at a temperature of 130° C. and a hydrogen pressure of 50 kg/cm2G for 40 minutes and then at 160° to 170° C. and a hydrogen pressure of 60 to 70 kg/cm2G for 40 minutes. After cooled to room temperature, the catalyst is filtered off and isopropanol was removed at a reduced pressure. The residue was recrystallized from toluene to obtain 290 g of 4,4'-(perfluoroisopropylidene)dicyclohexanol in the form of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788327 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-41540affc4e949d2b1bfef045f4874a3 |
| Source note | uspto-grants-1988_11 |