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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230291생성일: 2026년 10월 26일

Water → tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyran

https://huagongshe.com/reaction/230291

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물tetrahydro-4-(4-iodophenyl)-2H-pyran-4-olHCID 57033480—
용매DimethylformamideHCID 6228—
생성물tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyranHCID 57762532—

반응 단계

Under an argon atmosphere, a solution of tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol (2.99 g) in anhydrous DMF (10 ml) was added dropwise to a suspension of sodium hydride (60 wt %) (432 mg) in anhydrous DMF (20 ml) at room temperature, and the resulting mixture was stirred at room temperature for 75 minutes. Methyl iodide (0.92 ml) was added dropwise to the reaction solution and the resulting mixture was stirred at room temperature for 8.5 hours. Water was added thereto and the resulting mixture was extracted twice with ethyl acetate. Organic layers were washed with saturated brine, and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=10/1) to obtain tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyran (2.87 g). NMR (H1, CDCl3): δ 1.90-2.02 (4H, m), 2.97 (3H, s), 3.80-3.88 (4H, m), 7.14 (1H, d, J=8.5 Hz), 7.70 (1H, d, J=8.5 Hz)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566724B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-ec2052f962eb4e3db4d1c5504c4b8a05
출처 메모uspto-grants-2009_07