HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2'-(Carboxymethoxy)-4'-(3-methyl-2-butenyloxy)-4-(2-propenyl)chalcone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | {2-Acetyl-5-[(3-methylbut-2-en-1-yl)oxy]phenoxy}acetic acid | HCID 13247580 | — |
| Reactant | 4-(Prop-2-en-1-yl)benzaldehyde | HCID 13291762 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2'-(Carboxymethoxy)-4'-(3-methyl-2-butenyloxy)-4-(2-propenyl)chalcone | HCID 54147825 | 29.6% |
Reaction Steps
To a solution of 834 mg of 2'-(1-carboxymethoxy)-4'-(3-methyl-2-butenyloxy)acetophenone and 500 mg of 4-(2-propenyl)benzaldehyde in 10 ml of ethanol was added 842 mg of potassium hydroxide, and the mixture was stirred for 20 minutes. After neutralization with dilute hydrochloric acid, the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate - n-hexane to give 360 mg of the title compound as a pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089654 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-fd288b1651bc4900b0bcbd1cefc78b8d |
| Source note | uspto-grants-1992_02 |