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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452722Generated: October 30, 2026

Methyl iodide → HCID 68663038, compound

https://huagongshe.com/reaction/452722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68664421HCID 68664421—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68663038HCID 6866303873%

Reaction Steps

To a mixture of [4-[5-(5-methyl-1,3,4-oxadiazol-2-yl)-1-benzofuran-3-yl]phenyl]methanol (193 mg, 0.630 mmol), tetrahydrofuran (3 mL) and N,N-dimethylformamide (3 mL) was added sodium hydride (60% in oil, 37.8 mg, 0.945 mmol) at room temperature, and the resulting mixture was stirred for 10 min. Iodomethane (0.0588 mL, 0.945 mmol) was added to the reaction mixture, and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/tetrahydrofuran=2/1), and crystallized from hexane/tetrahydrofuran to give the title compound (146 mg, yield 73%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-cdaf04f9cf064b0f9b7b1ebf0dbdf338
Source noteuspto-grants-2013_07