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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 538833Erstellt: 24. Oktober 2026

Cesium carbonate → 4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid

https://huagongshe.com/de/reaction/538833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt2-Chloro-4-fluorophenolHCID 74814—
Edukt2-Bromo-4-tert-butylbenzoic acidHCID 236352—
LösungsmittelTolueneHCID 1140—
Produkt4-Tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acidHCID 5768770872,2%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

In a pressure-vessel, a stirring mixture of 2-bromo-4-tert-butylbenzoic acid (1.00 g, 3.89 mmol) and 2-chloro-4-fluorophenol (860 mg, 620 μL, 5.87 mmol) in toluene (20 mL) was added Cs2CO3 (2.53 g, 7.78 mmol) followed by copper(I) triflate benzene complex (98 mg, 0.19 mmol). The sealed vessel was heated to 120° C. for 16 h. After cooling to room temperature, the reaction mixture was partitioned between 50 mL EtOAc and 50 mL H2O. The aqueous layer was acidified using 2.0 N HCl(aq) and re-extracted with EtOAc. The combined organic solution was dried over Na2SO4, filtered, and concentrated. The residue was purified via silica gel chromatography using 0-3% MeOH/CH2Cl2 to give the product, 4-tert-butyl-2-(2-chloro-4-fluorophenoxy)benzoic acid as a white solid (907 mg, 2.81 mmol) in 72% yield. LC/MS: m/z 323.2 (M+H)+ at 1.99 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865771B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-68ad4472b6044f849aa739bd398b4e11
Quellennotizuspto-grants-2014_10