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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323755생성일: 2026년 10월 25일

2-Hydroxy-5-(trifluoromethoxy)benzaldehyde → 2-(1-Phenylthiocycloprop-1-yl)oxy-5-(trifluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/323755

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
반응물(1-Iodocyclopropyl)(phenyl)sulfaneHCID 11000298—
촉매HCID 178418647HCID 178418647—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(1-Phenylthiocycloprop-1-yl)oxy-5-(trifluoromethoxy)benzaldehydeHCID 2158407827%

반응 조건

온도40 °C

반응 단계

Silver carbonate (1.2 g, 4.34 mmol) was added to a solution of 2-hydroxy-5-(trifluoromethoxy)benzaldehyde (0.5 g, 2.43 mmol) and (1-iodocycloprop-1-yl)phenylsulfide (Cohen T. and Matz J. R., J. Am. Chem. Soc. 1980, 102, 6902) (1.2 g, 4.34 mmol) in toluene (30 mL) and the mixture was stirred at 40° C. overnight. The mixture was cooled, diluted with ethyl acetate and filtered, washing well with ethyl acetate. The mixture was washed with aqueous sodium hydroxide, 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 (95:5), to give the title compound as a yellow oil (191 mg, 27%). 1H NMR (360 MHz, CDCl3) δ1.51-1.56 (2H, m), 1.44-1.48 (2H, m), 7.25-7.35 (7H, m), 7.69 (1H, d, J 2.0 Hz), and 10.26 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214846B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-a8adc5e8d0934517b8299d7ddcc3da30
출처 메모uspto-grants-2001_04