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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 3-Fluoro-4-nitrobenzaldehyde | HCID 3808120 | — |
| 반응물 | (2-(tert-Butoxy)-2-oxoethyl)triphenylphosphonium chloride | HCID 16211488 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (E)-3-(3-Fluoro-4-nitro-phenyl)-acrylic acid tert-butyl ester | HCID 66905416 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08153663B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-1842b8fe0572404eb61514a4d6062641 |
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| 출처 메모 | uspto-grants-2012_04 |
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