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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595014생성일: 2026년 10월 24일

Carbon Dioxide → 3-Bromo-2,5,6-trifluorobenzoic acid

https://huagongshe.com/ko/reaction/595014

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylamineHCID 7912—
반응물1-Bromo-2,4,5-trifluorobenzeneHCID 67597—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물3-Bromo-2,5,6-trifluorobenzoic acidHCID 1427882552.3%

반응 단계

Step (i) n-Butyllithium (2.5M in hexane, 10.5 mL, 1.1 eq.) was added dropwise over 15 min to a solution of diisopropylamine (4.0 mL, 1.2 eq.) in THF (25 mL) at 0° C. After stirring for 15 min, the LDA solution was added dropwise over 40 min to a solution of 2,4,5-trifluorobromobenzene (5.0 g, 24 mmol) in THF (50 mL) at −78° C. The solution was stirred for 10 min and then transferred to a slurry of dry ice (50 g) in diethylether (65 mL). The reaction was allowed to warm to rt and treated with 1M HCl. The phases were separated and the organic layer extracted with 0.5M NaOH. The basic extracts were acidified to pH 1 with 6M HCl and extracted with diethylether. The combined organic phases were dried over sodium sulfate and evaporated to yield 3-bromo-2,5,6-trifluorobenzoic acid as a white solid (3.2 g, 52%). Step (ii)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242987B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-f458c925287840249be13624f543e5b1
출처 메모uspto-grants-2016_01