HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Oxo-2H,6H-[1,3]dioxolo[4,5-g][1]benzopyran-7-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 6,7-methylenedioxy-2-oxo-1-benzopyran-3-carboxylate | HCID 13193685 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 6-Oxo-2H,6H-[1,3]dioxolo[4,5-g][1]benzopyran-7-carboxylic acid | HCID 13193686 | 44% |
Reaction Steps
To a suspension of ethyl 6,7-methylenedioxy-2-oxo-1-benzopyran-3-carboxylate (0.26 g) in methanol (20 ml), 2N KOH (1.5 ml) was added, followed by stirring at room temperature for 2 hours. The reaction mixture was poured into water and acidified with hydrochloric acid; the resulting crystal was collected by filtration to yield 6,7-methylenedioxy-2-oxo-1-benzopyran-3-carboxylic acid (0.1 g, 44%), which was then recrystallized from N,N-dimethylformamide-water to yield yellow prisms having a melting point of 279°-280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716944 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-f12408e8bbe2489f8ca498b623c787ca |
| Source note | uspto-grants-1998_02 |