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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19152Generated: October 26, 2026

3-Cyanophenol → (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester

https://huagongshe.com/reaction/19152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-CyanophenolHCID 13394—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMethyl but-2-ynoateHCID 141019—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl esterHCID 6689504776%

Reaction Steps

To a stirred mixture of 3-hydroxy-benzonitrile (3.30 g, 0.028 mol) and methyl-2-butynoate (5.40 g, 0.055 mol) in tetrahydrofuran (50 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (4.20 g, 0.028 mol) slowly. After addition was complete the mixture was stirred at reflux for 6 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 mixture was filtered and evaporated and the residue dried under high vacuum which afforded (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester as an oil (4.60 g, 76%) and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-fb3e6c940794475996d3ab2a68d25e21
Source noteuspto-grants-2010_06