Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diallyl ether | HCID 11194 | — |
| Reactant | HCID 22998800 | HCID 22998800 | — |
| Solvent | Diethylene Glycol Monoethyl Ether | HCID 8146 | — |
| Product | HCID 67925638 | HCID 67925638 | 75% |
Reaction Steps
140 grams of the diallyl ether of indane bisphenol was placed into a one liter round bottom flask containing a magnetic stir bar and dissolved in 210 grams of 2-(2-ethoxyethoxy) ethanol. The solution was deoxygenated by bubbling dry argon gas through the solution for 15 minutes, and then a reflux condenser was attached. The solution was refluxed for 6 hours under an inert atmosphere. The solvent was removed by vacuum distillation between 60° and 62° C., and the product was collected between 210° and 214° C. as a light yellow, viscous liquid (13.3 Pa). Diallyl indane bisphenol was so viscous that the condenser on the still has to be heated with a hot air gun so that the product could flow into the collection flask; 110 grams of diallyl indane bisphenol were isolated (75% yield overall).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988785 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-e21923663c15421cbd338e5b72fbf7cc |
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| Source note | uspto-grants-1991_01 |
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