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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230291Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/230291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukttetrahydro-4-(4-iodophenyl)-2H-pyran-4-olHCID 57033480—
LösungsmittelDimethylformamideHCID 6228—
Produkttetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyranHCID 57762532—

Reaktionsschritte

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)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566724B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-ec2052f962eb4e3db4d1c5504c4b8a05
Quellennotizuspto-grants-2009_07