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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253664Erstellt: 26. Oktober 2026

Ethanol → Benzoic acid, 2-fluoro-5-(trifluoromethyl)-, ethyl ester

https://huagongshe.com/reaction/253664

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
Edukt2-Fluoro-5-(trifluoromethyl)benzoyl ChlorideHCID 2734880—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzoic acid, 2-fluoro-5-(trifluoromethyl)-, ethyl esterHCID 4631138792,3%

Reaktionsschritte

To a solution of 2-fluoro-5-(trifluoromethyl)benzoyl chloride (5.0 g, 22.0 mmol) in THF (25 mL) was added Et3N (3.1 mL, 22.0 mmol) followed by EtOH (1.3 mL, 22.0 mmol). This mixture was stirred at ambient temperature for 1 h and quenched with saturated, aqueous NH4Cl (10 mL). The layers were separated and the aqueous layer was extracted with 3×10 mL EtOAc and the combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by column chromatography (SiO2, 60% hexanes in EtOAc) to give the title compound (4.8 g, 20.3 mmol, 92% yield). 1H NMR (300 MHz, CDCl3) δ ppm 1.42 (t, J=7.1 Hz, 3H), 4.43 (q, J=7.1 Hz, 2H), 7.23-7.34 (m, 1H), 7.74-7.82 (m, 1H), 8.23 (dd, J=6.3, 2.4 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872033B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-151415f39307487aba353940c1f410b6
Quellennotizuspto-grants-2011_01