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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48486Erstellt: 25. Oktober 2026

Ethanol → Ethyl 2-chloro-4-fluoro-5-nitrobenzoate

https://huagongshe.com/reaction/48486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
Edukt2-Chloro-4-fluoro-5-nitrobenzoic AcidHCID 7210828—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 2-chloro-4-fluoro-5-nitrobenzoateHCID 22508453—

Reaktionsschritte

First, 50 g (0.29 mol) of 2-chloro-4-fluorobenzoic acid was dissolved in 150 ml of hydrochloric acid at room temperature, to which a mixed acid of 28 ml (0.31 mol) of fuming nitric acid and 56 ml of concentrated sulfuric acid was added dropwise at 35° to 45° C. Then, the solution was stirred at 40° C. for 1 hour and poured into 250 ml of ice-water. The precipitated crystals were collected by filtration and recrystallized from a mixed solution of hexane and ethyl acetate, which afforded 55 g (0.25 mol) of 2-chloro-4-fluoro-5-nitrobenzoic acid. Then, 55 g (0.25 mol) of 2-chloro-4-fluoro-5-nitrobenzoic acid was dissolved in 50 ml of ethyl acetate, to which 33 g (0.28 mol) of thionyl chloride was added, and the mixture was heated under reflux for 3 hours and then allowed to stand for cooling to room temperature. Then, 20 ml of ethanol and 30 g of triethylamine were added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The solvent was distilled out, and the residue was purified by silica gel chromatography, which afforded 57 g (0.23 mol) of ethyl 2-chloro-4-fluoro-5-nitrobenzoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703503B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-ec0140a251b0413f87e0b245af03ffaf
Quellennotizuspto-grants-2004_03