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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19111Generated: October 29, 2026

Ethyl 2-butynoate → (E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-butynoateHCID 78043—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Ethoxy-2-fluorophenolHCID 66894508—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl esterHCID 66894779—

Reaction Steps

To a stirred mixture of 3-ethoxy-2-fluoro-phenol (6.00 g, 0.038 mol) and ethyl-2-butynoate (8.60 g, 0.077 mol) in tetrahydrofuran (50 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (5.80 g, 0.038 mol) slowly. After addition was complete the mixture was stirred at reflux for 7 h. Upon completion of the reaction the tetrahydrofuran was removed in vacuo and the residue was diluted in diethyl ether and washed first with 1N aqueous hydrochloric acid, then 10% aqueous sodium hydroxide solution, a saturated sodium chloride solution and dried over magnesium sulfate. The crude product, (E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester, was obtained as a brown oil (6.00 g, 58%) and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-8176dc49da14495abf623ed52a166703
Source noteuspto-grants-2010_06