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HRID 489921作成日:2026年10月23日

Piperidine → 4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one

https://huagongshe.com/ja/reaction/489921

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物3-Fluoro-p-anisaldehydeHCID 67696—
反応物4-PyridinylacetoneHCID 80552—
溶媒TolueneHCID 1140—
生成物4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-oneHCID 69373148393.2%

反応手順

A solution of 4-pyridylacetone (1.0 g, 7.4 mmol), 3-fluoro-p-anisaldehyde (1.25 g, 8.1 mmol), and piperidine (0.13 g, 1.5 mmol) in toluene (50 ml) was heated to reflux. After 18 hours, the reaction was cooled to room temperature and the solvent was removed under reduced pressure. The crude product (3.0 g) was purified by column chromatography (silica gel, 65:35 ethyl acetate/hexane) to give 4-(3-fluoro-4-methoxylphenyl) -3-pyridyl-3-butene-2-one as a pale yellow solid (1.60 g, 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06979686B1
出典データセットuspto-grants-2005_12
ORD IDord-f9ced75ef53c4362afa8e12efbbe0011
出典メモuspto-grants-2005_12