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HRID 1595474作成日:2026年10月27日

Piperonal → E-6-[2-(1,3-benzodioxol-5-yl)ethenyl]-4-(phenylmethoxy)-2H-pyran-2-one

https://huagongshe.com/reaction/1595474

反応式

関与物質

役割名称HCID仕込み量
反応物PiperonalHCID 8438—
反応物4-Benzyloxy-6-methyl-2H-pyran-2-oneHCID 2784449—
生成物E-6-[2-(1,3-benzodioxol-5-yl)ethenyl]-4-(phenylmethoxy)-2H-pyran-2-oneHCID 2170511439%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06288109B1
出典データセットuspto-grants-2001_09
ORD IDord-a8fec576f22745a7811992b2137fde6f
出典メモuspto-grants-2001_09