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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409381Generated: October 30, 2026

Ethylene Oxide → 5-(2-Hydroxyethyl)furan-2(3H)-one

https://huagongshe.com/reaction/2409381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTetrahydrofuranHCID 8028—
ReactantFuranHCID 8029—
ReactantButyllithiumHCID 178418339—
Product5-(2-Hydroxyethyl)furan-2(3H)-oneHCID 1167981654%

Reaction Steps

To a cooled solution of furan (3.40 g, 50.0 mmol) in THF (150 mL) was added n-BuLi (22 mL, 2.5M solution in hexane, 55.0 mmol) at 0° C. under inert gas atmosphere. The solution was allowed to warm to room temperature and stirred for 3 h. Then TMSCl (5.34 g, 50 mmol) was added dropwise at 0° C. and the solution was stirred for further 3 h at room temperature. Subsequently, the solution was again cooled to 0° C. and n-BuLi (22 mL, 2.5M solution in hexane, 55.0 mmol) was added a second time. After stirring for 3 h at room temperature ethyleneoxide (2.42 g, 55.0 mmol) was condensed by an acetone/dry ice condenser into the solution and the solution was stirred for further 12 h at room temperature. The mixture was quenched with aq NH4Cl, and then extracted with EtOAc and the combined organic layers were dried over Na2SO4 to afforded the desired product (5 g, 27.1 mmol, 54% over two steps) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815873B2
Source datasetuspto-grants-2014_08
ORD IDord-898d76b98ce24852b05e6954e9e98868
Source noteuspto-grants-2014_08