Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetophenonoxime | HCID 69185 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 3,5-Diacetoxybromobenzene | HCID 68648240 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Triacetylresveratrol | HCID 5962587 | — |
Reaction Steps
A 10 ml Schlenk tube equipped with a magnetic stirrer is charged with 218 mg (0.8 mmol) 3,5-diacetoxybromobenzene, 136 mg (0.84 mmol) 4-acetoxystyrene, 187 mg potassium carbonate (0.9 mmol) and 0.22 mg (0.1 mol %) of the acetophenon-oxim derived palladium catalyst CAS No. 32679-19-9 as used in Example 9. The tube was evacuated and flushed with argon three times and 1 ml de-aerated DMF was added under inert conditions. The reaction was carried out under stirring for 15 hours at 150° C. Work-up was conducted following the procedure of Example 4 and to give (E)-3,4′,5-triacetoxystilbene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820848B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-2407f36fd476426987f9eb0da100a3f0 |
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| Source note | uspto-grants-2010_10 |
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