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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814086Generated: October 25, 2026

Triethylamine → 5-Ethoxycarbonyl-2-trimethylsilylethynylpyridine

https://huagongshe.com/reaction/1814086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 6-chloronicotinateHCID 2799611—
SolventDimethylformamideHCID 6228—
Product5-Ethoxycarbonyl-2-trimethylsilylethynylpyridineHCID 2250439793%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 6-chloronicotinic acid ethyl ester (1.92 g) in N,N-dimethylformamide (1 ml), trimethylsilylacetylene (2.0 g), bistriphenylphosphine palladium dichloride (210 mg), cuprous iodide (60 mg) and triethylamine (1.2 g) were added successively and the mixture was stirred in a sealed tube at 100° C. for 2 hours. After cooling, the reaction solution was poured into a saturated aqueous sodium hydrogencabonate solution, extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 2.38 g of the desired product as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-23cb354fc7f34a738922fca5e6c3ffdd
Source noteuspto-grants-2005_04