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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414172Generated: November 2, 2026

Tetrahydrofuran → 6-Methoxy-2H-1-benzopyran-3(4H)-one

https://huagongshe.com/reaction/2414172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12344687HCID 12344687—
Product6-Methoxy-2H-1-benzopyran-3(4H)-oneHCID 14006911—

Reaction Steps

To a suspension of 2.0 g sodium hydride in 100 ml of dry tetrahydrofuran is added with stirring a solution of 20 g of trans-3-bromo-4-hydroxy-6-methoxy-3,4-dihydro-2H-[1]-benzopyran in 200 ml of dry tetrahydrofuran in a dropwise fashion. Afer 30 minutes stirring at room temperature, the reaction mixture is filtered through filter-cel and the solvent is removed in vacuo. The residue is dissolved in 100 ml of toluene, 1.0 g of anhydrous zinc iodide is added and the mixture is heated at 80° for 1 hour. The reaction mixture is filtered through 120 g of silica gel with methylene chloride as the eluent to afford a product which is recrystallized from ether to give 6-methoxy-2H-[1]-benzopyran-3-one, melting point 67°-72°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04721787
Source datasetuspto-grants-1988_01
ORD IDord-1eb9d9d502924806aafb5eb0490aa65a
Source noteuspto-grants-1988_01