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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1060133Erstellt: 26. Oktober 2026

Ethylamine → 3-Chloro-2-fluorobenzoic acid

https://huagongshe.com/reaction/1060133

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylamineHCID 6341—
Edukt3-Chloro-2-fluoro-6-(trimethylsilyl)benzoic acidHCID 18630211—
Produkt3-Chloro-2-fluorobenzoic acidHCID 30293184%
Produkt3-Chloro-N-ethyl-2-fluoro-6-(trimethylsilyl)benzamideHCID 18630098—

Reaktionsschritte

The trimethylsilyl ester of 3-chloro-2-fluorobenzoic acid (11.66 g) was prepared in 84% yield using the method described in Example 207. This ester (2.47 g) was converted to 0.45 g of 3-chloro-2-fluoro-6-(trimethylsilyl)benzoic acid in 18% yield using the method of Example 207. The crude product was converted to the acid chloride by the procedure of example b. The acid chloride was reacted with 70% aq ethylamine using General Method E1 to afford the title compound. Purification by flash chromatography (ethyl acetate/hexanes) followed by recrystallization from pentane gave 84 mg of the title compound as an off-white solid (18%). m.p. 96-97° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06521603B2
Quelldatensatzuspto-grants-2003_02
ORD IDord-ffb93792985d451dbf7491b2ae89d8cb
Quellennotizuspto-grants-2003_02