HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814086Generated: October 25, 2026
Triethylamine → 5-Ethoxycarbonyl-2-trimethylsilylethynylpyridine
https://huagongshe.com/reaction/1814086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 6-chloronicotinate | HCID 2799611 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Ethoxycarbonyl-2-trimethylsilylethynylpyridine | HCID 22504397 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875770B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-23cb354fc7f34a738922fca5e6c3ffdd |
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| Source note | uspto-grants-2005_04 |
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