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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505965Generated: November 3, 2026

Trimethylsilylacetylene → 5-[(Trimethylsilyl)ethynyl]pyrimidine

https://huagongshe.com/reaction/505965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-BromopyrimidineHCID 78344—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
SolventDiisopropylamineHCID 7912—
SolventEthyl AcetateHCID 8857—
Product5-[(Trimethylsilyl)ethynyl]pyrimidineHCID 1534966985%

Reaction Conditions

Temperature60 °C

Reaction Steps

Tetrakis(triphenylphosphine)palladium(O) (727 mg, 0.6 mmol) was added to a stirred, degassed suspension of 5-bromopyrimidine (5.0 g, 31.4 mmol) and copper(I)iodide (120 mg, 0.6 mmol) in toluene and diisopropylamine (1:1, 200 ml) under nitrogen. The reaction mixture was heated to 60° C., trimethylsilylacetylene (4.89 ml, 34.6 mmol) was added and the reaction mixture was stirred for 3 hours at 60° C. The reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate (200 ml) and washed with saturated aqueous ammonium chloride solution (3×100 ml). The organic layer was separated, dried over MgSO4 and concentrated in vacuo. The crude product was purified by flash column chromatography (5% ethyl acetate/heptane) to give 5-trimethylsilanylethynyl-pyrimidine as a pale brown solid, 4.71 g (85% yield). LC at 215 nm; Rt 2.07: 88%, m/z (ES+): 177 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781593B2
Source datasetuspto-grants-2010_08
ORD IDord-ed51dcd02f0d49728475eac21d451aa2
Source noteuspto-grants-2010_08