Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Dicyclopentadiene | HCID 6492 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 22568287 | HCID 22568287 | — |
| Product | endo-Dicyclopentadiene | HCID 15618652 | — |
Reaction Steps
To a reactor equipped with a stirrer, condenser, thermowell and heater add 1882 gms (20 moles) of phenol and 8 gms (0.4% based on total weight) of boron trifluoride etherate. Heat to 70° C. and add 132 gms (~1 mole) of a C10 diene stream containing mainly dicyclopentadiene and cyclopentadiene-isoprene codimers over a 20 minute (1200 s) period. Increase the temperature to 150° C. over a 3 hour (10,800 s) time period and hold for about 3 hours (10,800 s). Distill off unreacted phenol with a finishing temperature of 210° C. and less than 5 mm Hg. The recovered product is a dicyclopentadiene bisphenol with an average functionality of 2.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04394497 |
|---|
| Source dataset | uspto-grants-1983_07 |
|---|
| ORD ID | ord-453e6f6a20a0470a916869f950673b58 |
|---|
| Source note | uspto-grants-1983_07 |
|---|