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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594838Generated: October 30, 2026

Methyl iodide → HCID 58067201, compound

https://huagongshe.com/reaction/594838

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 numberUS09242986B2
Source datasetuspto-grants-2016_01
ORD IDord-194cac15f26f4e07b28dfb4e6660e06d
Source noteuspto-grants-2016_01