Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942534Generated: October 31, 2026

Methyl iodide → 1-Acetyl-6-bromo-3,3-dimethylindolin-2-one

https://huagongshe.com/reaction/1942534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant1-acetyl-6-bromo-3-methyl-1,3-dihydro-2H-indol-2-oneHCID 10825759—
SolventWaterHCID 962—
Product1-Acetyl-6-bromo-3,3-dimethylindolin-2-oneHCID 10826719—

Reaction Steps

To 1-acetyl-6-bromo-3-methyl-1,3-dihydro-2H-indol-2-one (9.5 g) were added NaH (1.57 g), methyl iodide (2.45 ml) and THF (70 ml) under ice-cooling, and the mixture was stirred at room temperature for 2 hours. After the reaction was complete, water was added to the reaction solution, and the mixture was extracted with ethyl acetate solution. This ethyl acetate solution was washed with water and an aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to give the title compound (5.2 g) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-6aae1b14ef714dce8814ba9c97231da7
Source noteuspto-grants-2013_03