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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108299Generated: October 30, 2026

Methyl iodide → 2-(Cyclopropyl-methoxy-methyl)-7-methoxybenzofuran

https://huagongshe.com/reaction/1108299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantCyclopropyl-(7-methoxybenzofuran-2-yl)-methanolHCID 18784867—
SolventTetrahydrofuranHCID 8028—
Product2-(Cyclopropyl-methoxy-methyl)-7-methoxybenzofuranHCID 18784860—

Reaction Steps

To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.52 g) in tetrahydrofuran (60 ml) under an atmosphere of nitrogen was added slowly a solution of cyclopropyl-(7-methoxybenzofuran-2-yl)-methanol (1.88 g) in tetrahydrofuran (15 ml). After stirring for 5 minutes, iodomethane (1.6 ml) was added and the mixture concentrated in vacuo. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml), the organic layer washed with water (100 ml), separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with dichloromethane afforded the title compound as a yellow gum (1.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066657
Source datasetuspto-grants-2000_05
ORD IDord-6db5ecc150054891ad615a26161b92a0
Source noteuspto-grants-2000_05