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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292737Generated: October 31, 2026

Methyl iodide → 5-Bromo-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/1292737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant5-Bromo-2-hydroxypyridineHCID 599528—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—

Reaction Steps

To a solution of 4.38 g of the product from Step A in DMP was added 81 g of cesium carbonate and 30 mL of methyl iodide. The mixture was stirred at ambient temperature overnight, diluted with ethyl acetate, extracted sequentially with two portions of saturated aqueous sodium bicarbonate and brine, dried over sodium sulfate, and concentrated. Purification by HPLC (silica gel, 60% ethyl acetate/hexane) gave the title compound. 1H NMR (500 MHz, CDCl3) δ 7.46 (d, 1H, J=2.7 Hz), 7.38 (dd, 1H, J=2.7, 9.8 Hz), 6.52 (d, 1H, J=9.8 Hz), 3.55 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238683B2
Source datasetuspto-grants-2007_07
ORD IDord-1d6d689610124c4482c405f39468c4a1
Source noteuspto-grants-2007_07