HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperonal → E-6-[2-(1,3-benzodioxol-5-yl)ethenyl]-4-(phenylmethoxy)-2H-pyran-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperonal | HCID 8438 | — |
| Reactant | 4-Benzyloxy-6-methyl-2H-pyran-2-one | HCID 2784449 | — |
| Product | E-6-[2-(1,3-benzodioxol-5-yl)ethenyl]-4-(phenylmethoxy)-2H-pyran-2-one | HCID 21705114 | 39% |
Reaction Steps
6-methyl-4-(phenylmethoxy)-2H-pyran-2-one (known) was reacted with piperonal in accordance with Method C described above under II to form E-6-[2-(1,3-benzodioxol -5-yl)ethenyl]-4-(phenylmethoxy)-2H-pyran-2-one: C21H16O5; yield 39%, melting point 150 to 152° C. (acetone). This condensation product was hydrogenated in accordance with Method A described above under I. For cleaning purposes the product was taken up in ethyl acetate, was extracted therefrom with 2 N potassium hydroxide solution and was precipitated from the latter by acidification: C14H12O5; yield 67%, melting point 200 to 201° C. (isopropanol/water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288109B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-a8fec576f22745a7811992b2137fde6f |
| Source note | uspto-grants-2001_09 |