Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932439Generated: October 30, 2026

Methyl iodide → HCID 68527197, compound

https://huagongshe.com/reaction/1932439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131729741HCID 131729741—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 68527197HCID 68527197—

Reaction Steps

To a solution of ethyl(2,5-difluoro-4-hydroxyphenyl)aminoacetate (1.1 g, 4.8 mmol) in DMF (25 mL) were added sodium bicarbonate (0.44 g, 5.2 mmol) and methyl iodide (1.69 mL, 28.6 mmol), and the resulting reaction solution was stirred for 2 days at room temperature. Water was added to the reaction mixture, and extracted with ethyl acetate. Once the ethyl acetate layer had been washed with water, the ethyl acetate layer was dried with anhydrous magnesium sulfate, and evaporated. The residue was dissolved in DMF (30 mL), and to this resulting solution were added potassium carbonate (0.72 g, 5.2 mmol) and 2-chloro-5-nitropyridine (0.79 g, 5.0 mmol). The reaction solution was stirred for 2.5 days at room temperature. Water was added to the reaction mixture, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, and dried over anhydrous magnesium sulfate. The solvent was then evaporated, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=8:1), to thereby yield 1.41 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188277B2
Source datasetuspto-grants-2012_05
ORD IDord-6d52c557b6fb4ea38ad604c6e1aae946
Source noteuspto-grants-2012_05