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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377629Generated: October 27, 2026

Ethylene Oxide → Ethyl 1-(3-butenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/2377629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(diethoxyphosphinyl)-5-hexenoateHCID 14217021—
CatalystEthanolHCID 702—
SolventBenzeneHCID 241—
ProductEthyl 1-(3-butenyl)cyclopropanecarboxylateHCID 1421702248%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of NaH (60% dispersion in mineral oil, 3.02 g, 75.5 mmol) in dry benzene (100 mL), at 22° C. and under nitrogen, was added dropwise ethyl 2-(diethoxyphosphoryl)hex-5-enoate with anhydrous EtOH (0.044 mL, 0.76 mmol) over 30 minutes. Stirred for 30 minutes, this reaction, cooled at 0° C. and attached with a dry ice/acetone condenser, was added via cannula ethylene oxide (12.7 g, 289.3 mmol), then refluxed at 50° C. for 5 hours. Quenched at 22° C. with 1N aqueous NH4Cl (100 mL), the reaction solution was extracted with Et2O (3×200 mL). The combined Et2O layers were washed with aqueous saturated NaHCO3 (100 mL), water (70 mL), brine (70 mL), dried over Na2SO4, filtered and concentrated. The residue was flash chromatographed on 120 g silica gel 60, eluting with 20-100% EtOAc/Hexane, to give the title product (5.07 g, 48%). LRMS (ESI) m/z 169.2 [(M+H)+; calcd for C10H17O2: 169.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470664B2
Source datasetuspto-grants-2008_12
ORD IDord-42a607674f884891912b0a25d7030abb
Source noteuspto-grants-2008_12