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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020773Generated: October 26, 2026

Ethyl Acetate → Ethyl 3-oxo-3-(oxolan-3-yl)propanoate

https://huagongshe.com/reaction/1020773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantMethyl oxolane-3-carboxylateHCID 10678263—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-oxo-3-(oxolan-3-yl)propanoateHCID 2283188138.4%

Reaction Steps

To a solution of lithium bis(trimethylsilyl)amide (1 M in hexanes; 100 mL) in THF (200 mL) at −78° C. was added dry ethyl acetate (10.8 g, 12 mL, 122.5 mmol) dropwise. After 30 min at −78° C., the mixture was treated with a solution of tetrahydro-furan-3-carboxylic acid methyl ester (6.0 g, 46.1 mmol) in THF (50 mL). After 4 h at −78° C., the reaction was quenched with satd. aq. NH4Cl, warmed to rt, and extracted with EtOAc (5×75 mL). The combined organic layers were washed with satd. aq. NaCl, dried, and concentrated to give a colorless oil. Chromatography on SiO2 (EtOAc/CH2Cl2) afforded the title compound (3.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716475B2
Source datasetuspto-grants-2014_05
ORD IDord-d8e878b4c7114f8eb8f1c400ff797d4f
Source noteuspto-grants-2014_05