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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503985Generated: November 3, 2026

Methyl iodide → 8-methoxy-1-methyl-3,4-dihydro-1H-quinolin-2-one

https://huagongshe.com/reaction/503985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3,4-Dihydro-8-methoxy-2(1H)-quinolinoneHCID 13375476—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product8-methoxy-1-methyl-3,4-dihydro-1H-quinolin-2-oneHCID 1338419696%

Reaction Steps

8-Methoxy-3,4-dihydro-1H-quinolin-2-one (15 g) was dissolved in DMF (150 ml), and 3.6 g of sodium hydride (60% in oil) was added under ice cooling. After the addition, stirring was carried out at room temperature until the generation of hydrogen stopped. The resulting mixture was cooled with ice water again, and 5.8 ml of methyl iodide was added dropwise, followed by stirring at room temperature overnight. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to thereby obtain 16.7 g (yield: 96%) of 8-methoxy-1-methyl-3,4-dihydro-1H-quinolin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777038B2
Source datasetuspto-grants-2010_08
ORD IDord-0ff5eaa87a1d47c9bb68144dbd36f2b9
Source noteuspto-grants-2010_08