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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3-Cyanophenylboronic acid | HCID 2734325 | — |
| Reactant | 3-[(Trifluoromethylsulfonyl)oxy]acrylic acid ethyl ester | HCID 86758106 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl (2E)-3-(3-cyanophenyl)-2-propenoate | HCID 5373498 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399627B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-fb42fb351bcb4c479abd111a9d69c398 |
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| Source note | uspto-grants-2002_06 |
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