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Piperidine → 4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 3-Fluoro-p-anisaldehyde | HCID 67696 | — |
| 反応物 | 4-Pyridinylacetone | HCID 80552 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one | HCID 69373148 | 393.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06979686B1 |
| 出典データセット | uspto-grants-2005_12 |
| ORD ID | ord-f9ced75ef53c4362afa8e12efbbe0011 |
| 出典メモ | uspto-grants-2005_12 |