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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19388Generated: October 25, 2026

Potassium Carbonate → (E)-3-(benzooxazol-4-yloxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-butynoateHCID 78043—
Reactant1,3-Benzoxazol-4-olHCID 13720697—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(benzooxazol-4-yloxy)-but-2-enoic acid ethyl esterHCID 66895566100.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred mixture of benzooxazol-4-ol (0.388 g, 2.87 mmol), ethyl-2-butynoate (1.93 g, 17.2 mmol) a catalytic amount of 4-dimethylaminopyridine and potassium carbonate (0.595 g, 4.30 mmol) in tetrahydrofuran (20 mL) was placed in a sealed tube and heated at 80° C. for 2 h. The reaction mixture was filtered and the filtrate was collected and concentrated in vacuo. The resulting residue was purified by ISCO column chromatography (Silicycle 40 g, 2% to 15% ethyl acetate/hexanes) which afforded (E)-3-(benzooxazol-4-yloxy)-but-2-enoic acid ethyl ester (710 mg, 100%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-a6e7976868214a29b3b7aa30f68365d0
Source noteuspto-grants-2010_06