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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992326Generated: October 31, 2026

Trimethylsilylacetylene → 2-(Trifluoromethyl)-5-[(trimethylsilyl)ethynyl]pyrimidine

https://huagongshe.com/reaction/1992326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantAluminumHCID 5359268—
Reactant2-(Trifluoromethyl)pyrimidin-5-yl trifluoromethanesulfonateHCID 86615160—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-(Trifluoromethyl)-5-[(trimethylsilyl)ethynyl]pyrimidineHCID 6735090795.5%

Reaction Steps

2-(Trifluoromethyl)pyrimidine-5-yl trifluoromethanesulfonate (0.45 g, 1.5 mmol) and dry triethylamine (1.0 mL) were mixed in a screw-cap vial. The solution was purged with dry argon for 10 minutes. Trimethylsilylacetylene (0.43 mL, 3.0 mmol), finely ground CuI (0.010 g, 0.05 mmol) and PdCl2(PPh3)2 (0.020 g, 0.030 mmol) were added. The vial was sealed and heated in an aluminum block at 80° C. After stirring for 5 hours the volatiles were evaporated at room temperature (the product sublimes at 35-40° C./10 mbar). The black residue was taken up in EtOAc (20 mL) and concentrated with silica (about 5 to 10 g) to dryness. Flash chromatography on silica with EtOAc/heptane (1:30) afforded 2-(trifluoromethyl)-5-[(trimethylsilyl)ethynyl]pyrimidine as a white solid (0.35 g, 95%), m.p. 75.5-76.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648992B2
Source datasetuspto-grants-2010_01
ORD IDord-8cf4269e0c8f43e782e1537c601f2bdf
Source noteuspto-grants-2010_01