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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 474577Erstellt: 24. Oktober 2026

Ammonium Chloride → 3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl ester

https://huagongshe.com/de/reaction/474577

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktEthyl (dimethoxyphosphinoyl)acetateHCID 67555—
Edukt2,4,6-TrifluorobenzaldehydeHCID 521845—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmitteltetrahydrofuran N,N-dimethylformamideHCID 21974620—
Produkt3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl esterHCID 5741277987%

Reaktionsschritte

To the solution of ethyl[bis(methyloxy)phosphoryl]acetate (1.980 mL, 11.99 mmol) in THF-DMF (60 mL, v/v=5:1) at 0° C. was added t-BuOK (1.458 g, 12.99 mmol) portion wise. The resultant mixture was stirred at room temperature for 30 minutes, then mixed with a solution of 2,4,6-trifluorobenzaldehyde (1.6 g, 9.99 mmol) in THF (10 mL) at 0° C. It was allowed to warm to room temperature and the mixture was stirred for 45 min. It was mixed with aqueous ammonium chloride and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified by a flash column chromatography to give the title compound as a pale yellow oil (2.0 g, 87% yield). LCMS: rt=3.52 min, [M+H+]=231.1

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637536B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e0957e9540054c5f81479c9091b0c6c2
Quellennotizuspto-grants-2014_01