HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2',4',6'-Trihydroxy3'-(2-propenyl)acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2',4',6'-Trihydroxy3'-(2-propenyl)acetophenone | HCID 14368078 | 41.5% |
Reaction Steps
In 15 ml of anhydrous tetrahydrofuran was dissolved 3.0 g of 2',4',6'-trihydroxyacetophenone, and 7.4 g of anhydrous potassium carbonate was added to the solution and the mixture was stirred at room temperature for 30 minutes. Then, 2.5 g of 3-bromo-1-propene was added to the mixture and reaction was carried out at room temperature for 3 hours. After the reaction, the reaction mixture was extracted with 500 ml of diethyl ether, and the solvent was removed from the extract by distillation. The obtained residue was recrystallized from benzene to obtain 1.5 g (yield=41.5%) of 2',4',6'-trihydroxy-3'-(2-propenyl)acetophenone in the form of a colorless prism.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106871 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-3fabc0dff25e41778d2397b75add0719 |
| Source note | uspto-grants-1992_04 |