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HRID 28605Erstellt: 24. Oktober 2026

Potassium Carbonate → 2-Bromo-4-chloro-1-(2,2,2-trifluoroethoxy)-benzene

https://huagongshe.com/de/reaction/28605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-Bromo-4-chlorophenolHCID 69670—
Edukt2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Bromo-4-chloro-1-(2,2,2-trifluoroethoxy)-benzeneHCID 22571484108%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 2-bromo-4-chloro-phenol (2.0 g, 9.6 mmol), trifluoro-methanesulfonic acid 2,2,2-trifluoro-ethyl ester (3.8 g, 16.4 mmol), potassium carbonate (8.0 g, 59 mmol), and N,N-dimethylformaldehyde (80 ml) was heated to 100° C. for 72 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure. The residue was treated with water (150 ml) and extracted with ethyl acetate (160 ml). The organic extract was dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4) to give 2-bromo-4-chloro-1-(2,2,2-trifluoro-ethoxy)-benzene (3.0 g, 100% yield). 1H NMR (acetone-d6) δ 4.80 (q, 2H, J=8.4 Hz, CH2), 7.28 (d, 1H, J=8.9 Hz, Ar), 7.45 (dd, 1H, J=8.9 Hz, J=2.5 Hz, Ar), 7.69 (d, 1H, J—2.5 Hz, Ar).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419984B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-5dfa535b15fa45bab30e6b895f399d6a
Quellennotizuspto-grants-2008_09