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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468538Generated: October 30, 2026

Methyl iodide → HCID 58067201, compound

https://huagongshe.com/reaction/468538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 46239167HCID 46239167—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 58067201HCID 58067201—

Reaction Steps

Crude 1-[2,2-bis(methyloxy)ethyl]-4-oxo-3-[(phenylmethyl)oxy]-1,4-dihydro-2-pyridinecarboxylic acid 22 obtained as above was dissolved in DMF (500 mL). To this solution was added NaHCO3 (50.5 g, 0.6 mole). The suspension was stirred vigorously with a mechanic stirrer while CH3I in TBME (2.0 M, 300 mL) was introduced by addition funnel over 30 minutes. After addition, the reaction was stirred overnight at room temperature. The reaction mixture was then diluted with EtOAc (˜1.5 L) and washed with water and brine. The organic layer was dried over anhydrous Na2SO4. Evaporation of solvents gave methyl 1-[2,2-bis(methyloxy)ethyl]-4-oxo-3-[(phenylmethyl)oxy]-1,4-dihydro-2-pyridinecarboxylate 23 as brown oil, which was used directly for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624023B2
Source datasetuspto-grants-2014_01
ORD IDord-5d1a6a85c02b4193b3f8676fd9ce8782
Source noteuspto-grants-2014_01