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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7197Erstellt: 23. Oktober 2026

Trimethylsilylacetylene → 1,4-Bis(trimethylsilylethynyl)-2,5-dimethoxybenzene

https://huagongshe.com/de/reaction/7197

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt1,4-Dibromo-2,5-dimethoxybenzeneHCID 231240—
KatalysatorCopper iodideHCID 83717—
LösungsmittelDiisopropylamineHCID 7912—
Produkt1,4-Bis(trimethylsilylethynyl)-2,5-dimethoxybenzeneHCID 1059257273,8%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

100 g (0.338 mol) of 1,4-dibromo-2,5-dimethoxybenzene, 7.12 g (0.01 mol) of bistriphenylphospine palladium dichloride and 1.93 g (0.01 mol) of copper iodide were put into a 1 litter 3-neck round-bottom flask equipped with a stirrer, a thermometer and a reflux condenser under an argon atmosphere, and dissolved in 600 ml of diisopropylamine. 99 g (1 mol) of trimethylsilylacetylene was then slowly added dropwise at room temperature, and stirred at 80° C. for 12 hours. When the reaction was completed, the reaction mixture was cooled down to room temperature, generated salt was filtered off, and then the solvent was removed under a reduced pressure. The residue was dissolved in chloroform, and resultant was washed with water several times and then dried with anhydrous magnesium sulfate, which was then filtered off. The solvent was removed, and the residue was recrystallized from ethyl acetate/hexane mixture to obtain pale yellow crystal, which was sufficiently dried in a vacuum oven at 40° C. to give 82.5 g (yield: 73%) of the desired product, and its melting point was 164° C.–165° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084231B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-055226509f2c42309f67211cf933f618
Quellennotizuspto-grants-2006_08