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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817920Generated: November 3, 2026

Water → Trimethyl((2-nitrophenyl)ethynyl)silane

https://huagongshe.com/reaction/1817920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductTrimethyl((2-nitrophenyl)ethynyl)silaneHCID 1133347096%

Reaction Steps

4 g (20 mmol) of ortho-bromonitrobenzene, 842 mg (1.2 mmol) of bis(triphenyl-phosphine)palladium(II) chloride and 230 mg (1.2 mmol) of copper(I) iodide were, under argon, initially charged in 40 ml of triethylamine. At room temperature, 2.95 g (30 mmol) of trimethylsilylacetylene were then added dropwise over a period of 10 min, and the mixture was stirred at room temperature for 2 days. The reaction mixture was poured into 50 ml of water and extracted three times with in each case 50 ml of diethyl ether, and the extracts were dried over sodium sulphate and concentrated. Column-chromatographic purification on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 3:1) gave 4.2 g (96% of theory) of trimethyl-(2-nitrophenyl-ethynyl)silane [log P (pH 2.3)=4.12].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598389B2
Source datasetuspto-grants-2009_10
ORD IDord-7ff16f9ba0e44e368e21d53d40c9fc6c
Source noteuspto-grants-2009_10