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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497487Generated: October 28, 2026

Hydrochloric Acid → Ethyl 3-oxooxane-4-carboxylate

https://huagongshe.com/reaction/497487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 4-(2-ethoxy-2-oxoethoxy)butanoateHCID 21362494—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
ProductEthyl 3-oxooxane-4-carboxylateHCID 2136249348%

Reaction Steps

A solution of 4-ethoxycarbonylmethoxybutyric acid ethyl ester (90%, 15.0 g, 61.9 mmol) in toluene (300 mL) was stirred at room temperature and treated over 5 min with a solution of potassium tert-butoxide in tetrahydrofuran (1.0 M, 74.2 mL, 74.2 mmol). The mixture was stirred at room temperature for 24 h, then was poured into 1 N hydrochloric acid. The phases were separated, and the aqueous phase was extracted with ether. The combined organic phases were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by flash column chromatography (5% ethyl acetate/hexanes) to provide the product as a pale yellow liquid (5.06 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949546B2
Source datasetuspto-grants-2005_09
ORD IDord-56426b1e43bc442e9b8b98f15632c61a
Source noteuspto-grants-2005_09