돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1690562생성일: 2026년 10월 27일

3-Fluoro-4-nitrobenzaldehyde → (E)-3-(3-Fluoro-4-nitro-phenyl)-acrylic acid tert-butyl ester

https://huagongshe.com/reaction/1690562

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-nitrobenzaldehydeHCID 3808120—
반응물(2-(tert-Butoxy)-2-oxoethyl)triphenylphosphonium chlorideHCID 16211488—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(3-Fluoro-4-nitro-phenyl)-acrylic acid tert-butyl esterHCID 6690541686%

반응 단계

To a suspension of (tert-butoxycarbonylmethyl)triphenylphosphonium chloride (1.6 g, 3.9 mmol; [35000-37-4]) in tetrahydrofuran (10 ml) was added potassium tert-butoxide (0.44 g, 3.9 mmol). After stirring for 15 min 3-fluoro-4-nitrobenzaldehyde (0.60 g, 3.5 mmol; [160538-51-2]) was added. After 1.5 h the suspension was poured on water, the phases were separated and the aqueous phase extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash-chromatography using a gradient of n-heptane:tert-butyl methyl ether (100:0 to 80:20) to give the title compound (804 mg, 3.01 mmol; 86%) as light brown solid. MS: m/e=194.0 [M−C4H9O+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153663B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-1842b8fe0572404eb61514a4d6062641
출처 메모uspto-grants-2012_04