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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31972생성일: 2026년 10월 25일

2-Fluoroaniline → Methyl 4-amino-3-fluoro-2-((2-fluorophenyl)amino)-5-nitrobenzoate

https://huagongshe.com/reaction/31972

반응식

참여 물질

역할이름HCID투입량
반응물2-FluoroanilineHCID 9584—
반응물Benzoic acid, 4-amino-2,3-difluoro-5-nitro-, methyl esterHCID 2759749—
용매DichloromethaneHCID 6344—
생성물Methyl 4-amino-3-fluoro-2-((2-fluorophenyl)amino)-5-nitrobenzoateHCID 7165112552%

반응 조건

온도140 °C

반응 단계

4-Amino-2,3-difluoro-5-nitro-benzoic acid methyl ester 4 (1.50 g, 6.46 mmol) is suspended in xylenes (7.5 mL) and 2-fluoro-phenylamine (6.24 mL, 64.6 mmol) is added. The reaction mixture is stirred at 140° C. under N2. After stirring for 6 days, the reaction is complete. The reaction mixture is cooled to room temperature and diluted with methylene chloride and filtered through a silica gel plug eluting with methylene chloride (1L) to give an orange filtrate. The filtrate is concentrated to dryness and then triturated with diethyl ether to yield a bright yellow solid. The trituration is repeated. The yellow solid is collected to yield 1.08 g (52%) of the pure desired product. MS APCI (−) m/z 322 (M−1) detected.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425637B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a218f4c9703d410ba27d4755e5577c3e
출처 메모uspto-grants-2008_09