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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Methyl-2-nitropyridin-3-ol | HCID 84801 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Methoxy-6-methyl-2-nitropyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710043B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-7a2eaececb364ff2a5f9ab703baeee30 |
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| Source note | uspto-grants-2014_04 |
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