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HRID 29499作成日:2026年10月24日

Hydrochloric Acid → (2-Amino-5-chlorophenyl)-pyridin-4-yl methanone

https://huagongshe.com/ja/reaction/29499

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-CyanopyridineHCID 7506—
反応物4-ChloroanilineHCID 7812—
反応物Sodium HydroxideHCID 14798—
反応物Boron TrichlorideHCID 25135—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2-Amino-5-chlorophenyl)-pyridin-4-yl methanoneHCID 1021453875%

反応手順

A solution of 4-chloroaniline (2.0 g, 16 mmol) in 30 mL of TCE was added drop wise to a solution of BCl3 (1M in DCM) (24 ml, 24 mmol) with ice bath cooling, over a period of 15 min and the reaction mixture stirred at that temperature for an additional 10 min. 4-Cyanopyridine (2.0 g, 19 mmol) and AlCl3 (3.0 g, 22 mmol) were added with ice-water cooling. The solution was allowed to warm to room temperature and stirred for 30 min. The resulting solution was refluxed at 160° C. for 4 h and stirred at room temperature overnight. The reaction mixture was then treated with 30 mL of 3N HCl and the mixture was refluxed at 110° C. for 1.5 h. The reaction mixture was allowed to cool down to room temperature and the solution was adjusted to pH12 with 6N NaOH and then diluted water and DCM. The resulting two layers were separated and the aqueous layer was extracted with DCM three times and the organic layers combined and dried over sodium sulfate. After removal of the solvent, the resulting solid was washed with ether to yield (2-amino-5-chloro-phenyl)-pyridin-4-yl-methanone (2.8 g, 75%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420055B2
出典データセットuspto-grants-2008_09
ORD IDord-9de0386cbc414af1b5378a748a7a4251
出典メモuspto-grants-2008_09