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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19138Generated: October 29, 2026

Ethyl 2-butynoate → HCID 66894459, compound

https://huagongshe.com/reaction/19138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-butynoateHCID 78043—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Bromo-2-fluorophenolHCID 18401257—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66894459HCID 6689445969.5%

Reaction Steps

To a stirred mixture of 3-bromo-2-fluoro-phenol (19.5 g, 0.102 mol) and ethyl-2-butynoate (22.0 g, 0.196 mol) in tetrahydrofuran (100 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (15.6 g, 0.102 mol) slowly. After addition was complete the mixture was stirred at reflux for overnight. 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 mixture was filtered and evaporated, and the residue dried under high vacuum which afforded (E)-3-(3-bromo-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester as a brown oil (21.5 g, 69%) and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-47b3ae0f39024205804574097f350538
Source noteuspto-grants-2010_06