戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 483482作成日:2026年10月26日

Water → N-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline

https://huagongshe.com/reaction/483482

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物N-Phenyl-1-(phenylmethyl)-4-piperidinamineHCID 70865—
反応物3-Butoxyprop-2-enoyl chlorideHCID 53439772—
溶媒Diisopropyl EtherHCID 7914—
生成物N-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)anilineHCID 5421063698%

反応条件

温度70 °C

反応手順

To a mixture of N-(1-benzyl-4-piperidinyl)aniline (1.8 g), diisopropyl ether (20 ml) and triethylamine (0.87 g) is added dropwise a solution of β-n-butoxyacrylic acid chloride (1.4 g) in diisopropyl ether (5 ml) with stirring and heating at 70° C. After completion of dropwise addition, the mixture is further stirred with heating at the same temperature for 0.5 hour. After cooling, water is added to the reaction mixture and the mixture is subjected to extraction with ethyl acetate. The extract is washed with water and dried over magnesium sulfate. The solvent is distilled off under reduced pressure and the resulting residue is purified by silica gel column chromatography to give N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)-aniline (2.6 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225402
出典データセットuspto-grants-1993_07
ORD IDord-961a585b2cfe4d859a4bab81ab32d461
出典メモuspto-grants-1993_07