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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 729362Erstellt: 25. Oktober 2026

Ethanol → Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl ester

https://huagongshe.com/reaction/729362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktOxalyl chlorideHCID 65578—
EduktSodium BicarbonateHCID 516892—
Edukt2,4,5-Trifluoro-3-methoxybenzoic acidHCID 2733970—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl esterHCID 277438798,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 2,4,5-trifluoro-3-methoxybenzoic acid (2.513 g, 12.19 mmol) in dichloromethane (50 mL) at 0° C. is treated with oxalyl chloride (5.4 mL, 61.9 mmol) followed by N,N-dimethylformamide (4 drops). The mixture is stirred at 0° C. for 5 minutes and then at room temperature for 2.5 hours. The mixture is concentrated to near dryness and then co-evaporated from benzene. The resulting acid chloride is diluted with dichloromethane (50 mL), cooled to 0° C., and then anhydrous ethanol (7.30 mL, 124 mmol) is added dropwise. The resulting solution is stirred at room temperature for 4.5 hours, poured into saturated NaHCO3 solution, and extracted with dichloromethane. The combined organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to afford the title compound as a light yellow liquid (2.82 g). 1H NMR (CDCl3): δ 7.47 (ddd, 1H), 4.39 (q, 2H), 4.05 (s, 3H), 1.40 (t, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07582627B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-276df7c94fad4fc6a9035df569eaef47
Quellennotizuspto-grants-2009_09