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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230291Generated: October 25, 2026

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

https://huagongshe.com/reaction/230291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttetrahydro-4-(4-iodophenyl)-2H-pyran-4-olHCID 57033480—
SolventDimethylformamideHCID 6228—
Producttetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyranHCID 57762532—

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566724B2
Source datasetuspto-grants-2009_07
ORD IDord-ec2052f962eb4e3db4d1c5504c4b8a05
Source noteuspto-grants-2009_07