Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12636318 | HCID 12636318 | — |
| Reactant | HCID 21270126 | HCID 21270126 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21270179 | HCID 21270179 | — |
Reaction Steps
6,7-Methylenedioxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one [cp. Nippon Kagaku Zasshi 85, 793 (1964), Agr. Biol. Chem. (Tokyo) 32, 740 (1968) and Angew. Chem. 93, 129 (1981)] (2.0 g) is dissolved in dimethylformamide (15 ml) and K2CO3 (2.8 g) is added to the solution. While stirring, 2-bromoethylbutyrate (2.7 g) is dropped into the mixture. The content of the reaction flask is refluxed for 30 min. After cooling, water (50 ml) is added and the mixture is extracted with chloroform (3×30 ml), the extract washed with water (3×15 ml) and dried over Na2SO4. Chloroform is removed under reduced pressure and the residue is recrystallized from methanol. The product is dried in vacuo to constant weight to yield 6,7-methylenedioxy-3-[4-(1-ethoxycarbonyl-1-propyloxy)-phenyl]-4H-1-benzopyran-4-one, m.p. 119°-121°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04814346 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-c90afb2ae182468aba3110d2b5d51f89 |
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| Source note | uspto-grants-1989_03 |
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