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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130315Erstellt: 26. Oktober 2026

2,3,4,5-Tetrafluorobenzoyl chloride → Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate

https://huagongshe.com/reaction/130315

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
EduktPotassium ethyl malonateHCID 3446434—
EduktMagnesium ChlorideHCID 5360315—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—

Reaktionsschritte

Potassium ethyl malonate (3.66 g, 21.5 mmol), MgCl2 (2.44 g, 25.7 mmol) and TEA (2.05 g, 20.3 mmol) were mixed in acetonitrile (70 ml) at 10-15° C. for 2.5 hr. 2,3,4,5-tetrafluorobenzoyl chloride (2.00 g, 10.3 mmol) in acetonitrile (10 ml) was added at 0° C. over 15 min followed by a second addition of TEA (0.23 g, 2.3 mmol). After allowing to warm to RT, the mixture was stirred for 16 hr. After removal of volatiles in vacculo Toluene (30 ml) was added and removed in vacuo. Following the addition of toluene (60 ml), HCl 1.5 M (40 ml) was added cautiously, ensuring the temperature did not exceed 25° C. The organic fraction was washed with HCl 1.5 M (2×25 ml) and water (2×25 ml), dried over MgSO4 and reduced to a light orange oil in vacuo ([M+1]+265, 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381720B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-474bceeecd274ea987153a50a8377102
Quellennotizuspto-grants-2008_06