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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369294Generated: October 30, 2026

Triethylamine → HCID 11058212, compound

https://huagongshe.com/reaction/1369294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Propyne, 3-(chloromethoxy)-HCID 12241341—
ReactantHCID 54696216HCID 54696216—
SolventEthyl AcetateHCID 8857—
ProductHCID 11058212HCID 1105821282.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

6.4 g (20 mmol) of 4-hydroxy-5-methyl-6-(2-pyridyl)-3-(2,4,6-trimethylphenyl)-2-pyrone in 50 ml of ethyl acetate are introduced in the absence of moisture. 2.02 g (20 mmol) of triethylamine are added thereto at 20° C. and a solution of 2.1 g (20 mmol) of propargyloxychloromethane in 20 ml of ethyl acetate is added dropwise at 0° C. with cooling. The mixture is further stirred for 20 h at 20° C. and the reaction is followed by thin-layer chromatography. The solution is filtered off from the precipitated triethylamine hydrochloride with suction and washed with ethyl acetate. The combined mother liquors are washed twice, each time with 50 ml of half-saturated common salt solution, dried over magnesium sulfate and evaporated in vacuo. 8 g of crude product are obtained. 6.4 g (82% of theory) of 5-methyl-6-(2-pyridyl)-4-propargyloxymethoxy-3-(2,4,6-trimethylphenyl)-2-pyrone are obtained as an oil by flash chromatography on 500 g of silica gel 60 (35-70 μm) using toluene:acetone 20:1 as mobile phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576771B1
Source datasetuspto-grants-2003_06
ORD IDord-8252fa52d60245eead628b280ffd419a
Source noteuspto-grants-2003_06