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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276071Erstellt: 25. Oktober 2026

Iodobenzene → 3-Fluoro-4-methylbiphenyl

https://huagongshe.com/reaction/276071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodobenzeneHCID 11575—
Edukt4-Bromo-2-fluorotolueneHCID 171040—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-Fluoro-4-methylbiphenylHCID 1612750299,1%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Thirty milliliters of a 1.6-M-n-butyllithium hexane solution and a solution of 9.21 g of 4-bromo-2-fluorotoluene in 30 ml of tetrahydrofuran were added in this order to 30 ml of tetrahydrofuran which had been cooled to −78° C. in a nitrogen atmosphere, and the mixture was then stirred at −78° C. for 1 hour. A solution containing 6.64 g of zinc chloride which had been dehydrated through heat-melting under reduced pressure in 30 ml of tetrahydrofuran was added thereto at −78° C., and the mixture was stirred at room temperature for 1 hour. The reaction solution was added to a solution of 6.63 g of iodobenzene and 0.52 g of tetrakis(triphenylphosphine)palladium (0) in 30 ml of tetrahydrofuran at room temperature, and the mixed solution was stirred for 24 hours. The reaction solution was diluted with 300 ml of ethyl acetate, and the dilute solution was extracted with the addition of 10% hydrochloric acid. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried, and then concentrated. The residue was purified through silica-gel column chromatography (eluent: hexane) to give 6.00 g of oily 3-fluoro-4-methylbiphenyl.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352985B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-58153a43c1514d19abfc18e4b3526ee6
Quellennotizuspto-grants-2002_03