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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1852215생성일: 2026년 10월 26일

Triethylamine → (E)-3-(4-fluorophenyl)acryloyl azide

https://huagongshe.com/reaction/1852215

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물4-Fluorocinnamic acidHCID 1530234—
용매BenzeneHCID 241—
생성물(E)-3-(4-fluorophenyl)acryloyl azideHCID 8668326690.7%

반응 단계

To a solution of (E)-3-(4-fluorophenyl)acrylic acid (25 g, 150 mmol) in benzene (120 mL) was added triethylamine (30.5 g, 301 mmol) followed by DPPA (41.4 g, 150 mmol) at room temperature. The reaction mass was stirred at the same temperature for 18 h. The solvent was evaporated under reduced pressure and the residue was diluted with water and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to get crude compound. The crude compound was purified by conventional column chromatography (Silica gel, 60-120 mesh) using 10% ethyl acetate in pet ether as mobile phase to get the desired compound as a white solid (26 g, 90%). 1H NMR (400 MHz, CDCl3): δ ppm 7.73-7.69 (d, J=16 Hz, 1H), 7.55-7.51 (m, 2H), 7.11-7.07 (m, 2H), 6.36-6.32 (d, J=16 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957203B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-e3a102e078fc4d61a4814000f61cd73f
출처 메모uspto-grants-2015_02