HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenyl Acetate → Triacetylresveratrol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenyl Acetate | HCID 13410 | — |
| Reactant | Pentapotassium Triphosphate | HCID 61695 | — |
| Reactant | 3,5-Diacetoxy Styrene | HCID 11310559 | — |
| Reactant | Bis(adamantan-1-yl)(butyl)phosphane | HCID 11371790 | — |
| Product | Triacetylresveratrol | HCID 5962587 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A 10 ml Schlenk tube equipped with magnetic stirrer was charged with 119 mg (0.7 mmol) of 4-acetoxychlorobenzene, 200 mg (0.84 mmol, 1.2 eq) of 3,5-diacetoxystyrene, 177 mg (0.84 mmol, 1.2 eq) of potassium triphosphate, 5 mg of diadamantyl-n-butylphosphine (0.014 mmol, 2 mol %) and 3.7 mg (0.003 mmol, 0.5 mol %) of tris(dibenzylideneacetone)-dipalladium chloroform complex. The tube was evacuated and flushed with argon three times, and 2 ml of de-aerated DMAc was added under inert conditions. The reaction was carried out under stirring for 15.5 hours at 120° C. Work-up of the reaction mixture following the procedure of Example 5 gave (E)-3,4′,5-triacetoxystilbene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820848B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-d2ca098f09834c4cad0be0b1f98ebcb7 |
| Source note | uspto-grants-2010_10 |