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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458278Erstellt: 24. Oktober 2026

Hexane → (4-Bromo-2,6-dichlorophenyl)(trimethyl)silane

https://huagongshe.com/de/reaction/458278

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktTrimethylsilyl triflateHCID 65367—
Edukt5-Bromo-1,3-dichloro-2-iodobenzeneHCID 4574491—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(4-Bromo-2,6-dichlorophenyl)(trimethyl)silaneHCID 2307169190%

Reaktionsschritte

The 2,6-Dichloro-4-bromoiodobenzene (4.48 g, 12.7 mmol) was dissolved in diethyl ether (50 ml). To the solution was then added dropwise a hexane solution of n-butyl lithium (1.56 M, 8.2 ml) at −78° C. At the same temperature, the mixture was then stirred for 1 hour. To the mixture was then added dropwise trimethylsilyl trifluoromethanesulfonate (3.2 ml, 16.5 mmol). The mixture was then stirred at −78° C. for 1 hour and at room temperature for 30 minutes. After the quenching of the reaction with water, the mixture was then extracted with ether. The resulting organic phase was then dried over magnesium sulfate. The solvent was then distilled off. The crude product thus obtained was then distilled under reduced pressure in a glass tube oven so that it was purified to obtain 3,5-dichloro-4-trimethylsilyl-bromobenzene (3.39 g; yield: 90%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189790B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-659b6c0f088d4756b4a3d2c014389226
Quellennotizuspto-grants-2007_03