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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452707Generated: October 30, 2026

Butanoic acid, 4-chloro-4-oxo-, ethyl ester → Ethyl 3-[5-(2,3-dihydro-1-benzofuran-5-yl)-1,3,4-oxadiazol-2-yl]propionate

https://huagongshe.com/reaction/452707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanoic acid, 4-chloro-4-oxo-, ethyl esterHCID 84648—
Reactant5-(2,3-dihydro-1-benzofuran-5-yl)-1H-tetrazoleHCID 178419807—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[5-(2,3-dihydro-1-benzofuran-5-yl)-1,3,4-oxadiazol-2-yl]propionateHCID 6866448578.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-(2,3-dihydro-1-benzofuran-5-yl)-1H-tetrazole (4.40 g, 23.38 mmol) in pyridine (50 mL) was added ethyl 4-chloro-4-oxobutyrate (4.62 g, 28.06 mmol), and the resulting mixture was stirred at room temperature for 30 min and at 100° C. for 3.5 hr. After cooling, the reaction mixture was diluted with ethyl acetate, washed with water, 1M hydrochloric acid, 1M aqueous sodium hydroxide solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=95/5-0/100) and recrystallized from hexane/ethyl acetate to give the title compound (5.27 g, yield 78%) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-da56a99d1e994698986b97684f31b8c9
Source noteuspto-grants-2013_07