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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521824생성일: 2026년 10월 25일

Sulfuric Acid → 4-Cyclopropyl-2-fluoro-1-iodobenzene

https://huagongshe.com/reaction/521824

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Potassium IodideHCID 4875—
반응물4-Cyclopropyl-2-fluoroanilineHCID 20100071—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-Cyclopropyl-2-fluoro-1-iodobenzeneHCID 5959662371.28%

반응 단계

To a stirred mixture of 4-cyclopropyl-2-fluoroaniline (1.63 g, 10.78 mmol) in water (20 mL) at 0° C. was added concentrated sulfuric acid (8.6 mL, 15.0 eq.) dropwise, while keeping the temperature constant at 0° C. A solution of sodium nitrite (781.0 mg, 11.32 mmol, 1.05 eq.) in water (2.7 mL) was added and stirred for 5 minutes. This resulting reaction mixture was then added to a solution of potassium iodide (3.76 g, 22.64 mmol, 2.1 eq.) in water (9.7 mL), and the reaction mixture was stirred at 60° C. for 3 h. DCM (400 mL) was added to the cooled reaction. The biphasic layers were separated, and the aqueous layer was extracted with DCM (2×150 mL). The combined organic layers were washed with saturated aqueous Na2S2O4, water, and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude residue was purified via flash column chromatography eluted with 100% heptane to give 2.01 g (71.28%) of 4-cyclopropyl-2-fluoro-1-iodobenzene as a clear oil. 1H NMR (400 MHz, CDCl3) δ 7.57 (dd, J=8.0, 6.9 Hz, 1H), 6.76 (dd, J=9.4, 1.9 Hz, 1H), 6.64 (dd, J=8.2, 1.9 Hz, 1H), 1.94-1.77 (m, 1H), 1.09-0.95 (m, 2H), 0.79-0.56 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328106B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-ef60e1037b2b482693fd680652bb4f53
출처 메모uspto-grants-2016_05