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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443110Generated: November 2, 2026

Triphenylphosphine → 2-Methyl-5-trimethylsilanylethynyl-thiazole-4-carbonitrile

https://huagongshe.com/reaction/1443110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-2-methylthiazole-4-carbonitrileHCID 849383—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product2-Methyl-5-trimethylsilanylethynyl-thiazole-4-carbonitrileHCID 68538507—

Reaction Conditions

Temperature70 °C

Reaction Steps

5-Bromo-2-methyl-thiazole-4-carbonitrile (4.8 g, 23.6 mmol) was suspended in 50 ml triethyl amine. Trimethylsilylacetylene (4.64 g, 47.3 mmol), triphenylphosphine (186 mg, 0.7 mmol) and bis(triphenylphosphine)palladium(II)chloride (0.83 g, 1.18 mmol) were added and this mixture was evacuated and purged with argon several times to remove oxygen from the solution. Copper(I)iodide (45 mg, 0.24 mmol) was added and the reaction mixture was stirred at 70° C. for 5 hrs. The residue was taken up in water, extracted three times with ethyl acetate and several times with water. The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by chromatography on silica gel (heptane/ethyl acetate 90:10->1:1 gradient). The desired product was obtained as a black solid (4.1 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659401B2
Source datasetuspto-grants-2010_02
ORD IDord-7d3bfd896b1a405289e86edc6d6d7c1d
Source noteuspto-grants-2010_02