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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629235Generated: October 30, 2026

Triethylamine → 2-Bromo-5-((trimethylsilyl)ethynyl)pyrimidine

https://huagongshe.com/reaction/629235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Bromo-5-iodopyrimidineHCID 22507583—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-5-((trimethylsilyl)ethynyl)pyrimidineHCID 5751676170%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Bromo-5-iodopyrimidine (1.2 g, 4.2 mmol) was dissolved under nitrogen in 25 ml THF. Bis-(triphenylphosphine)-palladium(II)dichloride (300 mg, 420 μmol, 0.1 equiv.), ethynyltrimethylsilane (540 mg, 0.77 ml, 5.48 mmol, 1.3 equiv.), triethylamine (0.85 g, 1.17 ml, 8.4 mmol, 2 equiv.) and copper(I)iodide (40 mg, 210 μmol, 0.05 equiv.) were added and the mixture was stirred for 4 hours at 50° C. The reaction mixture was cooled and evaporated to dryness. The crude product was purified by flash chromatography on silica gel, eluting with an ethyl acetate:heptane gradient 0:100 to 40:60. The desired 2-bromo-5-trimethylsilanylethynyl-pyrimidine (0.75 g, 70% yield) was obtained as a yellow solid, MS: m/e=255/257 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315498B2
Source datasetuspto-grants-2016_04
ORD IDord-3ebc3d65e753428bb1b91b582e3d55ba
Source noteuspto-grants-2016_04