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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641110Generated: November 1, 2026

1-Bromo-4-nitrobenzene → Trimethyl((4-nitrophenyl)ethynyl)silane

https://huagongshe.com/reaction/641110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
ProductTrimethyl((4-nitrophenyl)ethynyl)silaneHCID 429609970%

Reaction Steps

A mixture of p-bromonitrobenzene (2.02 g, 10 mmol), bis(triphenylphosphine)palladium(II) chloride (0.2 g, 0.3 mmol), and copper(1) iodide (0.05 g, 0.3 mmol) in 40 ml of N,N-diisopropylamine was degassed by freeze/pump/thaw technique (three times). Trimethylsilylacetylene (1.2 g, 12 mmol) was added and the mixture was refluxed for 12 hours. After removal of amine by rotary evaporation, the residue was dissolved in CH2Cl2 and washed with water. The organic layer was dried (Na2SO4), filtered, and rotary evaporated. The residue was purified by column chromatography (EtOAc/hexanes, 1:10) to afford 4-(trimethylsilylethynyl)nitrobenzene (1.53 g, 70%). (Procedure adapted from Takahashi, S; Kuroyama, Y; Sonogashira, K; Hagihara, N. Synthesis, 1980, 627.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07695912B1
Source datasetuspto-grants-2010_04
ORD IDord-7ffa4e2129ec4f7c85a4bc5acfdf5883
Source noteuspto-grants-2010_04