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HRID 639741作成日:2026年10月25日

Water → 4-hydroxy-3-[3-[3-(cyanomethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/639741

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PiperidineHCID 8082—
反応物2-(3-Formylphenoxy)acetonitrileHCID 4766998—
反応物3-Acetyl-4-hydroxy-2H-chromen-2-oneHCID 54677403—
溶媒ChloroformHCID 6212—
生成物4-hydroxy-3-[3-[3-(cyanomethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-oneHCID 7618402557.8%

反応手順

In 5 ml of chloroform were dissolved 0.57 g of 3-acetyl-4-hydroxy-2H-1-benzopyran-2-one, 0.45 g of 3-(cyanomethoxy)benzaldehyde and 0.20 g of piperidine, and the solution was heated under refluxing for 1 hour and 30 minutes while water was removed with a Soxhlet's extractor filled with a molecular sieve. After cooling to room temperature, the reaction mixture washed successively with 10% hydrochloric acid and an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated. Precipitated crystals were washed with a mixture of 10 ml of dioxane and 10 ml of chloroform, and washed with 10 ml of t-butyl methyl ether to obtain 0.56 g of 4-hydroxy-3-[3-[3-(cyanomethoxy)phenyl]-1-oxo-2-propenyl]-2H-1-benzopyran-2-one [Compound No. (14d)] as a yellow crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691883B2
出典データセットuspto-grants-2010_04
ORD IDord-b8727b415aa34dfa8fb07d4d5e3889ed
出典メモuspto-grants-2010_04