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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 529703Erstellt: 25. Oktober 2026

Potassium Phosphate, Tribasic → Benzene, 1-ethenyl-3-methyl-5-(trifluoromethyl)-

https://huagongshe.com/reaction/529703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Edukt3-Bromo-5-methylbenzotrifluorideHCID 20467615—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorBis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+)HCID 12976736—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzene, 1-ethenyl-3-methyl-5-(trifluoromethyl)-HCID 6810581564,1%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To 1-bromo-3-methyl-5-(trifluoromethyl)benzene (500 mg, 2.51 mmol) was added THF (5 mL), aqueous tribasic potassium phosphate (2.0 M, 4.18 mL, 8.37 mmol), 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (387 mg, 2.51 mmol), palladium(II) acetate (47 mg, 0.209 mmol), and 1,1′-bis(di-t-butylphosphino)ferrocene (99 mg, 0.209 mmol). The system was flushed with nitrogen gas and was heated at 80° C. for 1 hour. The reaction was filtered and then diluted with ethyl acetate and water. The organic layer was dried over sodium sulfate, filtered and concentrated. The crude product was purified by preparative TLC to yield 1-ethenyl-3-methyl-5-(trifluoromethyl)benzene (300 mg, 1.61 mmol). 1H NMR (500 MHz, CDCl3) δ7.47 (s, 1H), 7.40 (s, 1H), 7.34 (s, 1H), 6.76 (m, 1H), 5.85 (d, J=17.6 Hz, 1H), 2.43 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346825B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-ef7916b892d54c78885a39a881e0db65
Quellennotizuspto-grants-2016_05