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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958754Generated: October 31, 2026

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

https://huagongshe.com/reaction/1958754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyltrimethylsilaneHCID 137936—
ReactantPyrimidine, 5-bromo-2-methoxy-HCID 139657—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Methoxy-5-((trimethylsilyl)ethynyl)pyrimidineHCID 6874227298.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-bromo-2-methoxypyrimidine (500 mg, 2.7 mmol) in ethyl acetate (2 mL) and water (0.2 mL) was added trimethylsilylethane (0.41 mL, 3 mmol), triethylamine (0.75 mL, 5.4 mmol), copper iodide (25 mg, 0.13 mmol) and bis(triphenylphosphine)palladium(II) dichloride (47 mg, 0.067 mmol). The solution was heated to 60° C. for 16 h. Ethyl acetate (100 mL) was added and the solution was washed with water (3×10 mL), dried over MgSO4 and treated with decolorizing charcoal. Ethyl acetate was removed in vacuo to give the title compound as a clear oil (547 mg, 97%). 1H NMR (400 MHz, CDCl3) δ 8.56 (s, 2H), 4.01 (s, 3H), 0.24 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410150B2
Source datasetuspto-grants-2013_04
ORD IDord-d12bb0f6e77d481898d35bb13a2dc50d
Source noteuspto-grants-2013_04