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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269869Generated: October 29, 2026

Furfuryl Alcohol → Ethyl fur-2-ylmethoxyacetate

https://huagongshe.com/reaction/2269869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuryl AlcoholHCID 7361—
ReactantEthyl bromoacetateHCID 7748—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
SolventDichloromethane ethylacetateHCID 21226138—
ProductEthyl fur-2-ylmethoxyacetateHCID 14746268—

Reaction Steps

Combine furfuryl alcohol (1 mL, 11.6 mmol) and tetrahydrofuran (20 mL). Add portionwise sodium hydride (0.57 g, 60% in oil, 14 mmol). After gas evolution ceases, add ethyl bromoacetate (1.3 mL, 11.7 mmol). Heat to reflux. After 2.5 hours cool to ambient temperature. After 18 hours, partition the reaction mixture between ethyl acetate and water. Separate the aqueous layer and extract twice with ethyl acetate. Combine the organic layers and extract with saturated aqueous sodium chloride solution, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 1% ethyl acetate/dichloromethane to give ethyl fur-2-ylmethoxyacetate: Rf=0.62 (silica gel, 5% ethyl acetate/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329392B1
Source datasetuspto-grants-2001_12
ORD IDord-f6ab3fbd2c5f4a6a962578c4e10ab001
Source noteuspto-grants-2001_12