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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370866Generated: October 31, 2026

Water → 5-Methoxy-2-methylpyridine

https://huagongshe.com/reaction/2370866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product5-Methoxy-2-methylpyridineHCID 13358777—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 60% NaH (in mineral oil) (18.27 g, 0.458 mol, Aldrich, India) in DMSO (66 mL, Spectrochem., India) at 0° C., was added 6-methylpyridin-3-ol (25.0 g, 0.229 mol) dissolved in DMSO (100 mL) drop wise over a period of 15 min. After complete addition, the reaction mixture was stirred at 0° C. for 40 min. Methyl iodide (29.5 mL, 0.458 mol, Spectrochem, India) was added and the reaction mixture was stirred at rt for 2 h. The reaction with water and Et2O (1:1, 200 mL). The organic layer was separated and aqueous layer was back extracted with Et2O (75 mL×3). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated to give the title compound as a dark brown gummy oil. 1H NMR (400 MHz, CDCl3) δ ppm 8.19 (d, J=2.8 Hz, 1H), 7.12-7.05 (m, 2H), 3.83 (s, 3H), 2.49 (s, 3H). MS (ESI, positive ion) m/z: 124.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-695548adc2da4e75856db561c990ed17
Source noteuspto-grants-2014_04