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HRID 439554作成日:2026年10月25日

3-Chloro-4-hydroxy-5-methoxybenzaldehyde → 2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide

https://huagongshe.com/reaction/439554

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-hydroxy-5-methoxybenzaldehydeHCID 29622—
反応物Acetamide, 2-cyano-N-phenyl-HCID 69296—
触媒PiperidineHCID 8082—
溶媒EthanolHCID 702—
生成物2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilideHCID 5418123874.1%

反応手順

To a solution of 5-chlorovanillin (728 mg, 3.9 mmol) and cyanoacetanilide (625 mg, 3.9 mmol) in ethanol (20 ml) were added 3 drops of piperidine, and the resulting mixture was refluxed for 2 hours. After cooling to room temperature, the resulting solid was filtered and washed with ethanol: water (1: 1) to give the objective 2-cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide (950 mg, 74% in yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05514711
出典データセットuspto-grants-1996_05
ORD IDord-ab545d1684904c21bbf62432b3ba8d21
出典メモuspto-grants-1996_05