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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500556생성일: 2026년 10월 24일

2-Chloroaniline → 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid

https://huagongshe.com/ko/reaction/500556

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloroanilineHCID 7240—
반응물DiisopropylamineHCID 7912—
반응물5-Bromo-2,3,4-trifluorobenzoic acidHCID 11118637—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acidHCID 2186699182%

반응 조건

온도-78 °C

반응 단계

To a solution of i-Pr2NH (25.0 mL, 178 mmol) in THF (200 mL) at 0° C. was added n-BuLi (71.0 mL, 178 mmol, 2.5 M solution in hexanes). After stirring for 15 minutes, this solution was cooled to −78° C. 2-Chloroaniline (12.7 mL, 118 mmol) was added. After vigorous stirring for 10 minutes, a solution of 5-bromo-2,3,4-trifluorobenzoic acid (14.95 g, 58.63 mmol) in THF (30 mL) was added. The dry-ice bath was removed, and the reaction mixture was stirred for 2 hours at room temperature. The mixture was concentrated, treated with 10% aqueous HCl (120 mL), extracted with EtOAc, dried over MgSO4, filtered, and concentrated to give the crude solid which was triturated with boiling CH2Cl2 (125 mL). The yellow solids were filtered, and dried in vacuo to give the desired product (17.4 g, 82%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772234B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-763cfd38f53343b4988c556c53be055a
출처 메모uspto-grants-2010_08