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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358945Generated: November 1, 2026

Methyl iodide → HCID 18180140, compound

https://huagongshe.com/reaction/1358945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Methoxy-5-nitrophenyl)pyridineHCID 14451969—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 18180140HCID 18180140—

Reaction Steps

A solution of 4-(2-methoxy-5-nitrophenyl)pyridine (D36) (3.4 g, 14.8 mmol) in acetone (150 ml) was treated with excess iodomethane (5 ml) and the mixture stirred at room temperature overnight. The precipitated quaternary salt was filtered off, washed with acetone and dried, giving 5.02 g. This was dissolved in 1:1 ethanol:water (230 ml) and treated portionwise at room temperature, under argon, with sodium borohydride (1.23 g, 32.4 mmol). The mixture was stirred for 1 h at room temperature then potassium carbonate (10 g) was added and the organic layer was separated from the aqueous phase, which was back-extracted with ethyl acetate. The organic phases were combined and dried (Na2SO4) and evaporated under reduced pressure to give the title compound (D37) as an orange oil, which slowly crystallised (3.05 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599904B2
Source datasetuspto-grants-2003_07
ORD IDord-1b11caaee7fd4daab2d8aa3519c7482b
Source noteuspto-grants-2003_07