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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184899Generated: October 31, 2026

Potassium Phosphate, Tribasic → Ethyl (2E)-3-(3-cyanophenyl)-2-propenoate

https://huagongshe.com/reaction/2184899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactant3-[(Trifluoromethylsulfonyl)oxy]acrylic acid ethyl esterHCID 86758106—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl (2E)-3-(3-cyanophenyl)-2-propenoateHCID 537349880%

Reaction Steps

To a solution of ethyl (E)-3-{[(trifluoromethyl)sulfonyl]-oxy}-2-propenoate (390 mg, 1.49 mmol) in 5 ml anhydrous dioxane was added potassium phosphate (474 mg, 2.24 mmol), 3-cyanophenyl boronic acid (217 mg, 1.49 mmol), and tetrakis (triphenylphosphine)palladium(0) (43 mg, 0.038 mmol). Reaction mixture was heated to reflux and stirred overnight. Mixture was filtered through a pad of Celite, diluted with 50 ml ethyl acetate, washed with 2×50 ml water, 2×50 ml saturated brine solution, dried over magnesium sulfate, filtered and concentrated in vacuo. Residue was chromatographed on silica gel using 5% EtOAc in hexane as the eluent to give ethyl (E) 3-(3-cyanophenyl)-2-propenoate (240 mg, 71%) as a clear yellow oil after drying. H1NMR (CDCl3): 1.2-1.32 (t, 3H); 2.547 (s, 3H); 4.18-4.24 (m, 2H); 6.113 (s, H); 7.47-7.725 (m, 4H). NOE confirmed stereo orientation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399627B1
Source datasetuspto-grants-2002_06
ORD IDord-fb42fb351bcb4c479abd111a9d69c398
Source noteuspto-grants-2002_06