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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370829Generated: November 1, 2026

Methyl iodide → 3-Methoxy-6-methyl-2-nitropyridine

https://huagongshe.com/reaction/2370829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Methyl-2-nitropyridin-3-olHCID 84801—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product3-Methoxy-6-methyl-2-nitropyridineHCID 2727965—

Reaction Steps

To a stirred mixture of 6-methyl-2-nitropyridin-3-ol (5 g, 0.032 mol, Sigma Aldrich) in DMF (50.0 mL) was added K2CO3 (6.72 g, 0.048 mol, S.d.fine chemicals, India). The reaction mixture was stirred for 30 min at room temperature. MeI (9 mL, 0.14 mol, Spectrochem, India) was then added at room temperature, and the reaction mixture was stirred overnight. After completion of the reaction (monitored by TLC, 30% EtOAc in hexane), the reaction mixture was quenched with ice water, following which the solid product precipitated. The solid was collected by filtration and washed with n-hexane to give the title compound. 1H-NMR (400 MHz, DMSO-d6): δ 7.88 (d, J=8.4 Hz, 1H), 7.64 (d, J=8.8 Hz, 1H), 3.92 (s, 3H), 2.44 (s, 3H). MS (ESI, positive ion) m/z: 169 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-7a2eaececb364ff2a5f9ab703baeee30
Source noteuspto-grants-2014_04