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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500537Generated: October 30, 2026

Potassium Carbonate → 2-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,2-dihydro-pyridine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/500537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantEthyl 2-oxo-1,2-dihydropyridine-4-carboxylateHCID 22625086—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,2-dihydro-pyridine-4-carboxylic acid ethyl esterHCID 24851701—

Reaction Steps

The title compound of example 18.1 (32 g, 191 mmol) and potassium carbonate (132 g, 957 mmol) were stirred in dimethylformamide (350 mL) at room temperature. Diisopropylethylamine (10 mL, 57 mmol) was added via a syringe, followed by 2-(trimethylsilyl)ethoxymethyl chloride (44.0 mL, 249 mmol). The reaction was stirred at room temperature and diisopropylethylamine (56.6 mL, 325 mmol) was added over 5 hours via a pressure equalized addition funnel. The reaction was then stirred overnight at room temperature. When TLC analysis showed that the reaction was complete the reaction mixture was diluted with ethyl acetate and washed four times with water and once with brine. The organic phase was dried over magnesium sulfate, filtered and concentrated. The residue was chromatographed on silica gel in 5-40% ethyl acetate in hexanes to purify the desired product (80%, trace amount of o-alkylated product observed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772235B2
Source datasetuspto-grants-2010_08
ORD IDord-f2da74112d484b2c99a2a6ba496b1a5f
Source noteuspto-grants-2010_08