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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580845생성일: 2026년 10월 24일

Diethyl Ether → 2-Cyclopropoxy-5-(trifluoromethoxy)benzaldehyde

https://huagongshe.com/ko/reaction/580845

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물TributylstannaneHCID 5948—
반응물1-(Cyclopropyloxy)-2-iodo-4-(trifluoromethoxy)benzeneHCID 11759692—
반응물HCID 178418416HCID 178418416—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
용매Potassium FluorideHCID 522689—
생성물2-Cyclopropoxy-5-(trifluoromethoxy)benzaldehydeHCID 21584076—

반응 조건

온도50 °C

반응 단계

A solution of 2-cyclopropoxy-5-(trifluoromethoxy)iodobenzene (Description 8, 0.344 g, 1 mmol) in toluene (2.5 mL) was degassed with bubbling nitrogen for 10 min. Tetrakis(triphenylphosphine)palladium (0) (15 mg) was added, the mixture was degassed with bubbling nitrogen for a further 5 min., then carbon monoxide was bubbled through the mixture for 10 min. The mixture was warmed to 50° C. and a solution of tributyl tin hydride (0.3 mL, 1.1 mmol) in toluene (5 mL) was added at a rate of 2 mL/h. via a syringe pump, maintaining carbon monoxide bubbling throughout. The mixture was cooled, diluted with ether (20 mL) and aqueous potassium fluoride solution (50%) was added. The mixture was stirred at room temperature overnight, filtered and the layers were separated. The organic layer was dried (MgSO4), and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with hexane/Et2O (80:20), to give the title compound as a colourless oil. 1H NMR (360 MHz, CDCl3) δ 0.86 (4H, m), 3.82-3.9 (1H, m), 7.42 (2H, m), 7.62 (1H, d, J 2.5 Hz), and 10.36 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05919781
출처 데이터셋uspto-grants-1999_07
ORD IDord-91770ec491f444149f0593533a433d61
출처 메모uspto-grants-1999_07