HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,9-dimethoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-hydroxy-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one | HCID 20380221 | — |
| Product | 2,9-dimethoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one | HCID 20380226 | — |
Reaction Steps
Dry methanol was saturated at 0° with gaseous hydrogen chloride. A sample of 0.576g. (2.46 mmoles) of 2-hydroxy-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one was dissolved in the resultant solution, and the dark reaction was allowed to proceed at room temperature for 1 hour. The solvent was evaporated and the residue was taken up in ethyl acetate/benzene, 1:4 and filtered through 50 g. silica, eluting with the same solvent system. Fractions containing the product, which is first eluted, were combined and evaporated to give pure 2,9-dimethoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one as a white solid. Recrystallization from methanol afforded an analytical sample of this product, mp 131-132°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130568 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-1e8989e6bfe44c98b8391fd2f5877959 |
| Source note | uspto-grants-1978_12 |