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HRID 236881作成日:2026年10月27日

Benzaldehyde → 4-(2-Phenylethenyl)pyridine

https://huagongshe.com/reaction/236881

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物PiperidineHCID 8082—
反応物Sodium HydroxideHCID 14798—
反応物4-MethylpyridiniumHCID 3434378—
溶媒IsopropanolHCID 3776—
生成物4-(2-Phenylethenyl)pyridineHCID 101576—

反応手順

To 67.5 parts of the 4-picolinium quaternary salt as in Example 13 but without the acid salt was added 100 parts isopropanol, 32.5 parts benzaldehyde, and one part piperidine. The resulting solution was boiled at reflux two hours, 100 parts 40% sodium hydroxide added, and the heating continued for two hours. The cooled mixture was extracted with chloroform, and the organic phase evaporated to dryness to yield a residue that was recrystallized from methanol-water to give 21 parts 4-styrylpyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04158093
出典データセットuspto-grants-1979_06
ORD IDord-34760d1e90e14ea3aa3e2fc44893f46d
出典メモuspto-grants-1979_06