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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432240Generated: October 26, 2026

Triethylamine → 5-Ethoxycarbonyl-2-trimethylsilylethynylpyridine

https://huagongshe.com/reaction/1432240

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 numberUS07612070B2
Source datasetuspto-grants-2009_11
ORD IDord-195ec3d6d5a24f11a0425ac0ed895c16
Source noteuspto-grants-2009_11