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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939166Generated: October 30, 2026

Toluene → 1-Methyl-6-nitroindoline

https://huagongshe.com/reaction/1939166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl iodideHCID 6328—
Reactant6-NitroindolineHCID 29757—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-6-nitroindolineHCID 12369047—

Reaction Steps

Potassium bis(trimethylsilyl)amide (67 ml of a 0.5M toluene solution) was added slowly to a stirred solution of 6-nitroindoline (5.0 g) in anhydrous tetrahydrofuran (200 ml) at -78° C. under a nitrogen atmosphere. Iodomethane (2.09 ml) was added then the reaction mixture was allowed to warm to room temperature then stirred overnight. Methanol (5 ml) was added then the solution was evaporated to dryness. The residue was dissolved in diethyl ether (300 ml), washed with water, saturated brine then dried (magnesium sulphate) and evaporated to dryness. The crude product was purified by column chromatography on silica using 10% ethyl acetate/petroleum ether (60-80)→30% ethyl acetate/petroleum ether (60-80) and the product crystallised from diethyl ether/petroleum ether (60-80) to afford 0.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696110
Source datasetuspto-grants-1997_12
ORD IDord-7050f3be52e54fcc98c5f41695d63839
Source noteuspto-grants-1997_12