HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359385Generated: November 1, 2026
Tetrahydropyran-2-methanol → HCID 18182313, compound
https://huagongshe.com/reaction/1359385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydropyran-2-methanol | HCID 7524 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 21942282 | HCID 21942282 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18182313 | HCID 18182313 | — |
Reaction Steps
Sodium hydride was added to a mixture of 456 mg of 2-benzyl-6-iodo-3-(methoxymethyloxy)pyridine, 122 mg of cuprous iodide and 3 ml of tetrahydropyran-2-methanol, followed by stirring at 90° C. for 3 hours. An aqueous ammonium chloride solution and ethyl acetate were added to the reaction solution, followed by stirring at room temperature for one hour. Then, the organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was removed. The residue was subjected to silica gel column chromatography using 15% ethyl acetate/hexane, to give 383 mg of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599917B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-3a3a20c3160140a389f7afc23408ed39 |
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| Source note | uspto-grants-2003_07 |
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