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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403681Generated: October 31, 2026

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

https://huagongshe.com/reaction/1403681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
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 TMSCI (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 numberUS08912209B2
Source datasetuspto-grants-2014_12
ORD IDord-af8aa3f706c242d59559c4c91e5ff054
Source noteuspto-grants-2014_12