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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2177312Erstellt: 26. Oktober 2026

Ethyl Acrylate → Ethyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoate

https://huagongshe.com/reaction/2177312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcrylateHCID 8821—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Bromo-3-(trifluoromethyl)phenolHCID 22277307—
KatalysatorPalladium ChlorideHCID 24290—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoateHCID 90442064—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 4-bromo-3-(trifluoromethyl)phenol (5 g, 20.75 mmol, 1.00 equiv), N,N-dimethylformamide (60 mL), ethyl prop-2-enoate (10.5 g, 104.88 mmol, 5.06 equiv), PdCl2 (370 mg, 2.09 mmol, 0.10 equiv), P(tolyl)3 (1.28 g, 4.21 mmol, 0.20 equiv), DIEA (16.25 g). The resulting solution was stirred for overnight at 90° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1/8). This resulted in 2.6 g (42%) of ethyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoate as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09067898B1
Quelldatensatzuspto-grants-2015_06
ORD IDord-40226ac7e7a3447c9b9553d7579d2e6e
Quellennotizuspto-grants-2015_06