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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 596054Erstellt: 25. Oktober 2026

Iodine → 4-Chloro-2-fluoro-6-iodobenzoic acid

https://huagongshe.com/reaction/596054

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktDimethylformamideHCID 6228—
Edukt4-Chloro-2-fluorobenzoic acidHCID 99152—
EduktIodo benzene diacetateHCID 12217721—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Chloro-2-fluoro-6-iodobenzoic acidHCID 118045935—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a 250 mL flask were added 4-chloro-2-fluorobenzoic acid (4 g, 22.92 mmol), Pd(OAc)2 (0.257 g, 1.146 mmol), iodobenzene diacetate (8.12 g, 25.2 mmol), iodine (6.40 g, 25.2 mmol) and DMF (60 mL). The solution was heated under a nitrogen atmosphere at 100° C. for 20 h. LCMS showed about half of 4-chloro-2-fluorobenzoic acid was converted to the product (LCMS retention time 0.98 min, no MH+ peak). After cooling to room temperature, the solution was diluted with EtOAc and washed three times with 1 N HCl. The aqueous layers were combined and extracted once with EtOAc. The organic layers were combined, dried over Na2SO4 and concentrated to give a dark brown oil (16.4 g, 42% pure), which was taken to the next step without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242996B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-3f19965fe351414d9c0e744a7d758022
Quellennotizuspto-grants-2016_01