Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2413821Erstellt: 23. Oktober 2026

Chlorotrimethylsilane → 2,2-Bis(4-trimethylsilylphenyl)hexafluoropropane

https://huagongshe.com/de/reaction/2413821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
Edukt2,2-Bis(4-bromophenyl)hexafluoropropaneHCID 13878551—
EduktAcetone cardiceHCID 18522661—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2,2-Bis(4-trimethylsilylphenyl)hexafluoropropaneHCID 13878552—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 4.62 g (0.1 mole) 2,2-bis(4-bromophenyl)hexafluoropropane in 75 ml of anhydrous tetrahydrofuran was added dropwise 28 ml (0.4 moles) of a 1.4 molar solution of n-butyllithium in hexane while the reaction mixture was cooled in a dry ice-acetone slush. The reaction mixture was stirred for one half hour at -78° C. A dropwise addition of chlorotrimethylsilane (5 ml, 0.04 moles) was then made to the reaction mixture at -78° C. The stirring slurry was allowed to come to ambient temperature over 16 hours. To the reaction mixture was added 100 ml hexane. The organic layer was washed with 2×150 ml saturated sodium chloride solution and 2×150 ml water. The organic layer was dried, filtered, and concentrated to yield the white crystalline product 2,2-bis(4-trimethylsilylphenyl)hexafluoropropane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04719258
Quelldatensatzuspto-grants-1988_01
ORD IDord-d765ba0c3e584a63bba42c489a0ab6ff
Quellennotizuspto-grants-1988_01