Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Dicyclopentadiene | HCID 6492 | — |
| Reactant | HCID 22568287 | HCID 22568287 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | endo-Dicyclopentadiene | HCID 15618652 | — |
Reaction Steps
To a reactor equipped as in Example 1-A were added 2823 gms (30 moles) of phenol and 16.1 gms of BF3 etherate in 20 gms of carbon tetrachloride. The mass was heated to 55° C. and 1201.2 gms (9.09 moles) of a 99.9% reactive C10 hydrocarbon stream consisting mainly of dicyclopentadiene and cyclopentadiene isoprene codimers was added over a 4 hour (14400 s) period. The temperature of the reaction mass was 80° C. after the hydrocarbon addition period. The reactor was heated to 150° C. over a 7 hour (25200 s) period and a vacuum distillation begun. The reaction was finished at 245° C. and 1 mm Hg. The resin had an equivalent weight of 187, a melt point of 115° C. and an average functionality of 2.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04394497 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-09d49f36ace74070bd5c5144268d3845 |
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| Source note | uspto-grants-1983_07 |
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