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HRID 29499생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-CyanopyridineHCID 7506—
반응물4-ChloroanilineHCID 7812—
반응물Sodium HydroxideHCID 14798—
반응물Boron TrichlorideHCID 25135—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(2-Amino-5-chlorophenyl)-pyridin-4-yl methanoneHCID 1021453875%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420055B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-9de0386cbc414af1b5378a748a7a4251
출처 메모uspto-grants-2008_09