戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1583653作成日:2026年10月27日

Potassium hydride → N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine

https://huagongshe.com/reaction/1583653

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium hydrideHCID 82127—
反応物2-Butene, 1-bromo-HCID 122414—
反応物N-(4-Chlorobenzyl)pyridin-3-amineHCID 10036347—
溶媒TetrahydrofuranHCID 8028—
生成物N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amineHCID 5451304154.7%

反応手順

A solution of 4.4 g of N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine dissolved in 50 ml of tetrahydrofuran was added to a suspension of 4 g of a 24.6% suspension of potassium hydride in oil in tetrahydrofuran. The mixture was allowed to stir at room temperature for approximately 30 minutes whereupon 4 g of 1-bromo-2-butene was added dropwise to the reaction mixture. The mixture was allowed to stir at room temperature overnight at which time the solution was evaporated to dryness. The residue was dissolved in dichloromethane and washed with water. The organic phase was dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum. The oil residue was chromatographed over silica gel. Fractions containing the major component were combined and the solvent was evaporated therefrom to provide 3 g of N-(2-butenyl)-N-[(4-chlorophenyl)methyl]-(3-pyridyl)amine as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04552960
出典データセットuspto-grants-1985_11
ORD IDord-c8d0fcc40cb94070ab4cc37bf1690e53
出典メモuspto-grants-1985_11