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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19294Generated: October 29, 2026

Phenol → (E)-3-phenoxy-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant3-Chloro-but-2-enoic acid ethyl esterHCID 282835—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-phenoxy-but-2-enoic acid ethyl esterHCID 535693989%

Reaction Conditions

Temperature23 °C

Reaction Steps

Potassium t-butoxide (11.9 g, 0.106 mol) was added to a stirred solution of phenol (7.86 g, 0.053 mol) in tetrahydrofuran (25 mL) at 23° C. under nitrogen and the reaction mixture was heated to reflux for 0.75 h. The reaction mixture was cooled to 23° C. and a solution of 3-chloro-but-2-enoic acid ethyl ester (prepared as in Example 191, 5.00 g, 0.034 mol) in tetrahydrofuran (40 mL) was added to the reaction mixture. The reaction mixture was refluxed for an additional 3 h. After this time, the mixture was concentrated in vacuo and the residue was diluted with water and extracted with diethyl ether. The organic layer was then washed with 5% aqueous sodium hydroxide solution followed by a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo to afford (E)-3-phenoxy-but-2-enoic acid ethyl ester (6.20 g, 89%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-fdf37033652245a194ae8e45f93182f4
Source noteuspto-grants-2010_06