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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7197Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1,4-Dibromo-2,5-dimethoxybenzeneHCID 231240—
CatalystCopper iodideHCID 83717—
SolventDiisopropylamineHCID 7912—
Product1,4-Bis(trimethylsilylethynyl)-2,5-dimethoxybenzeneHCID 1059257273.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084231B2
Source datasetuspto-grants-2006_08
ORD IDord-055226509f2c42309f67211cf933f618
Source noteuspto-grants-2006_08