돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38684생성일: 2026년 10월 24일

Nitrogen → (2'-Formyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester

https://huagongshe.com/ko/reaction/38684

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—
반응물[4-Methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic acid ethyl esterHCID 58120060—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물(2'-Formyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl esterHCID 86633171—

반응 조건

온도85 °C

반응 단계

A solution of [4-methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic acid ethyl ester (1.38 g, 4.32 mmol), 2-bromo-5-(trifluoromethyl)benzaldehyde (1.09 g, 4.32 mmol), and potassium carbonate (1.49 g, 10.8 mmol) in 2:1 DME:H2O was purged with N2 for 15 minutes. Tetrakis(triphenylphosphine)palladium(0) (0.499 g, 0.43 mmol) was added, and the reaction was purged with N2 for another 10 minutes, and then stirred at 85° C. overnight. The mixture was partitioned between EtOAc and H2O, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated, and the residue was purified by silica gel chromatography to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524748B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4a4fd1b10a664708a39f54ef10ebd3be
출처 메모uspto-grants-2013_09