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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19659Generated: October 29, 2026

Methyl iodide → 3-Iodo-4-methoxy-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/19659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 178516519HCID 178516519—
SolventDimethylformamideHCID 6228—
Product3-Iodo-4-methoxy-1-methylpyridin-2(1H)-oneHCID 22660656—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 2,4-dihydroxy-3-iodopyridine (1.0 eq), Cs2CO3 (2.0 eq), MeI (10.0 eq) and anhydrous DMF was stirred at 40° C. for 72 h, and then the DMF and remaining MeI were evaporated. The residue was treated with aqueous NaS2O3, and the mixture was extracted five times with CH2Cl2. The CH2Cl2 extracts were treated with MgSO4, filtered, and evaporated. The residue was recrystallized from hexanes/CH2Cl2 to give 1-methyl-3-iodo-4-methoxypyridin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745454B2
Source datasetuspto-grants-2010_06
ORD IDord-5a98d1f395ff43d281d83129ab2b6e90
Source noteuspto-grants-2010_06