HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl vinyl ketone → 1-(2H-1-Benzopyran-3-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(2H-1-Benzopyran-3-yl)ethanone | HCID 40067 | — |
Reaction Steps
1.22 g (10 mmol) of salicylaldehyde together with 0.66 g (10 mmol) of 3-oxo-l-butene are added at room temperature to a suspension of 0.14 g (1 mmol) of potassium carbonate in 50 ml of 2-butanone. The mixture is brought to reflux with stirring and this temperature is maintained for 4 hours. The procedure is then as in Example 1, stage A. The final chromatography is replaced by a recrystallization in hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04975454 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-55447b374b2745319a6f52cf6bf690b1 |
| Source note | uspto-grants-1990_12 |