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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359385Generated: November 1, 2026

Tetrahydropyran-2-methanol → HCID 18182313, compound

https://huagongshe.com/reaction/1359385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydropyran-2-methanolHCID 7524—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 21942282HCID 21942282—
SolventEthyl AcetateHCID 8857—
ProductHCID 18182313HCID 18182313—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-3a3a20c3160140a389f7afc23408ed39
Source noteuspto-grants-2003_07