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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43971Erstellt: 24. Oktober 2026

Trifluoroacetic acid → Ethyl 3-bromo-5-methylbenzoate

https://huagongshe.com/de/reaction/43971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktIsoamyl NitriteHCID 8053—
EduktPhosphinic AcidHCID 4124402—
EduktEthyl 2-amino-3-bromo-5-methylbenzoateHCID 54594338—
LösungsmittelEthanolHCID 702—
ProduktEthyl 3-bromo-5-methylbenzoateHCID 2008662487,3%

Reaktionsschritte

Ethanol (20 mL) was added to ethyl 2-amino-3-bromo-5-methylbenzoate obtained in Example (259d) (715 mg, 2.8 mmol). While the mixture was stirred, trifluoroacetic acid (0.82 mL, 11.1 mmol), isopentyl nitrite (649 mg, 5.5 mmol) and hypophosphorous acid (7.3 g, 55.4 mmol) were added under ice-cooling, followed by stirring at room temperature for 30 minutes. The reaction solution was diluted and extracted with ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=0/10, 2/8) to obtain 594 mg of the title compound as a light yellow oily substance (88%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536197B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c872ad6b93844f3591336c2f063f31e6
Quellennotizuspto-grants-2013_09