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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005405Generated: October 25, 2026

Ethyl Acetate → 5-Trimethylsilylethynyl-4-methyl-3-nitro-2-pyridone

https://huagongshe.com/reaction/1005405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-2-hydroxy-4-methyl-3-nitropyridineHCID 21706517—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product5-Trimethylsilylethynyl-4-methyl-3-nitro-2-pyridoneHCID 2170649196.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-bromo-4-methyl-3-nitro-2-pyridone (1.0 g, 2.8 mmol), trimethylsilylacetylene (1.2 mL, 8.5 mmol), bis(triphenylphosphine)Pd(II) chloride (0.100 g) and cuprous iodide (0.025 g) in DMF (4 mL) and triethylamine (2 mL) was heated at 90 ° C. in a sealed tube for 7 hours. Ethyl acetate was added, and the mixture was washed with water, dried, filtered and evaporated. Chromatography of the residue over silica gel (40% ethyl acetate/hexane) gave 5-trimethylsilylethynyl-4-methyl-3-nitro-2-pyridone (1.0 g, 2.7 mmol, 96%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054470
Source datasetuspto-grants-2000_04
ORD IDord-c9f1bf0a91384fa1b2adf3e397b54aee
Source noteuspto-grants-2000_04