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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19132Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → (E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester

https://huagongshe.com/reaction/19132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMethyl but-2-ynoateHCID 141019—
Reactant2-Fluoro-3-methoxyphenolHCID 40151763—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl esterHCID 6689525067.4%

Reaction Steps

To a stirred mixture of 2-fluoro-3-methoxy-phenol (3.88 g, 0.027 mol) and methyl-2-butynoate (5.97 g, 0.061 mol) in tetrahydrofuran (30 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (4.64 g, 0.030 mol) slowly. After addition was complete the mixture was stirred at reflux 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-(2-fluoro-3-methoxy-phenoxy)-but-2-enoic acid methyl ester (4.37 g, 63%) as a colorless oil and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-37a162c02fd34c2c8bf49af0de73d76d
Source noteuspto-grants-2010_06