HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Flavokavain A
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Xanthoxylin | HCID 66654 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Flavokavain A | HCID 235736 | 58% |
Reaction Steps
To a stirred solution containing 196 mg of 2'-hydroxy-4',6'-dimethoxyacetophenone and 150 mg of anisaldehyde in 3 ml of ethanol was added 50% aqueous potassium hydroxide (3 ml). After being stirred at room temperature for 3 days, the mixture was poured into 30 ml of cold water. The mixture was then extracted with three 30 ml portions of ethyl acetate. The combined ethyl acetate extracts were washed with water, dried over anhydrous sodium sulfate and then evaporated under reduced pressure to give a crystalline residue. Recrystallization of the residue from methanol gave 182 mg (50% yield) of 2'-hydroxy-4,4',6'-trimethoxychalcone as yellow needles: m.p. 110.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04605674 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-7b4b85d9d4c8416dbac5f909abb7e2ae |
| Source note | uspto-grants-1986_08 |