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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2113412생성일: 2026년 10월 25일

Aminopyralid → 4-Amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acid

https://huagongshe.com/reaction/2113412

반응식

참여 물질

역할이름HCID투입량
반응물AminopyralidHCID 213012—
반응물SelectfluorHCID 2724933—
용매WaterHCID 962—
생성물4-Amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acidHCID 2169664666.5%

반응 단계

A solution of 4-amino-3,6-dichloropyridine-2-carboxylic acid (1100 g, 5.31 mol), 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octanebis(tetrafluoroborate) (2100 g, 5.93 mol) in water (6000 mL) was warmed to 65° C. for six hours. After cooling to ambient temperature, the reaction mixture was stirred an additional 18 hours. The solution was concentrated and the resulting solid washed with 6 N hydrochloric acid (5×1000 mL) and dried to give 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylic acid (757 g, 3.53 mol. 58% purity). This crude material was added to methanol (3000 mL) which had been saturated with anhydrous hydrogen chloride and the reaction mixture was warmed to 45° C. for 2 hours. The solution was added with vigorous stirring to ice water (4000 mL) and the resulting solid collected. The crude ester was dissolved in ethyl acetate (1000 mL) and washed with saturated sodium bicarbonate solution (2×1000 mL), dried, and concentrated. The resulting solid was recrystallized from ethyl acetate/hexanes to give methyl 4-amino-3,6-dichloro-5-fluoropyridine-2-carboxylate (402.5 g, 1.67 mol), mp 128-131° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07432227B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-f297286f481c497dbbb33e5e8efc3b3c
출처 메모uspto-grants-2008_10