Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358952Generated: October 26, 2026

Methyl iodide → 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one

https://huagongshe.com/reaction/2358952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant6-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 14373281—
ReactantPotassium tert-butoxideHCID 23665647—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-oneHCID 6310614178%

Reaction Steps

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (339 mg, 1.50 mmol) in 15 ml dry DMF was added potassium tert-butylate (336 mg, 3.0 mmol). After the mixture was stirred for 30 min at room temperature, a solution of methyl iodide (426 mg, 3.0 mmol) in 5 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 100 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 7/3, Rf=0.21) gave 6-bromo-1-methyl-3,4-dihydro-1H-quinolin-2-one (281 mg, 1.17 mmol, 78%) as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685960B2
Source datasetuspto-grants-2014_04
ORD IDord-07a10a81436f41939437260f955e2692
Source noteuspto-grants-2014_04