HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Ethyl Ketone → 2H-1-Benzopyran, 3-acetyl-6-methoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2H-1-Benzopyran, 3-acetyl-6-methoxy- | HCID 42435 | — |
Reaction Steps
1.52 g (10 mmol) of 2-hydroxy™5-methoxybenzaldehyde, 0.66 g of 3-oxo-1-butene and 1.4 g (10 mmol) of potassium carbonate are added at room temperature and with magnetic stirring to 40 ml of 2-butanone. The mixture is brought to reflux with stirring and this temperature is maintained for 2 hours. After being cooled, the reaction medium is poured into 100 ml of water and extracted 3 times with 100 ml of diethyl ether. The organic phases are combined, washed to neutrality with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the organic phase is evaporated on a water bath under vacuum and the product recrystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04975455 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-3a20b39db2df49509f82f27bfdabe7c4 |
| Source note | uspto-grants-1990_12 |