HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-dimethyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][-1]benzopyran-7-one → 9-Methoxy-2,5-dimethyl-7h-furo[3,2-g]chromen-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-dimethyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][-1]benzopyran-7-one | HCID 20380224 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | 9-Methoxy-2,5-dimethyl-7h-furo[3,2-g]chromen-7-one | HCID 165305 | — |
Reaction Steps
A solution of 10.36 g (0.0422 mol) of 2,5-dimethyl-9-methoxy -2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one in 150 ml of diphenyl ether was treated with 6.0 g of 10% palladium on charcoal. The mixture was heated under reflux for 5.0 hrs, cooled, and filtered over celite. The catalyst was further washed with methanol, and the filtrate was then concentrated to remove the methanol. The residue was diluted with 1.5 1. of pet. ether and stirred overnight. The product was filtered, washed with pet. ether, dried, and passed through a silica column, eluting with ethyl acetate/benzene, 1:4, to yield pure 9-methoxy -2,5-dimethyl-7H-furo[3,2-g][1]benzopyran-7-one, m.p. 154°-155° (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130568 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-6bcfde82dd4c49a28b8073f4f0f1dae2 |
| Source note | uspto-grants-1978_12 |