HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360030Generated: October 25, 2026
Water → tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyran
https://huagongshe.com/reaction/1360030
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol | HCID 57033480 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tetrahydro-4-(4-iodophenyl)-4-methoxy-2H-pyran | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879837B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-b404ae9cb23d436bbf8b664368dda29f |
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| Source note | uspto-grants-2011_02 |
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