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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743396Generated: October 25, 2026

Triethylamine → 6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-one

https://huagongshe.com/reaction/1743396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantMethyl (methylthio)acetateHCID 85522—
ReactantProton spongeHCID 88675—
Reactant4-Methoxy-2,3-dimethylanilineHCID 11094809—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-oneHCID 2223807746%

Reaction Steps

To a solution of methyl (methylthio)acetate (40.8 mL, 317 mmol) in dichloromethane (1100 mL) was added sulfuryl chloride (26.6 mL, 331 mmol) at −78° C., and the mixture was stirred for 15 minutes. Further, a solution of 4-methoxy-2,3-dimethylaniline (41.7 g, 276 mmol) and proton sponge (62.1 g, 290 mmol) in dichloromethane (200 mL) was added dropwise over 1 hour and mixture was stirred at the same temperature for 1 hour. Triethylamine (43 mL, 380 mmol) was added, and the temperature was gradually raised to room temperature. After stirring at room temperature for 2 hours, water was added, the organic layer was washed with an aqueous saturated solution of sodium bicarbonate and saturated brine, dried over sodium sulfate, and the solvent was distilled off under reduced pressure. To the residue was added toluene (300 mL), and the mixture was stirred at reflux for 1 hour. The solvent was distilled off under reduced pressure, which was recrystallized from ethyl acetate to obtain 30.0 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008940B1
Source datasetuspto-grants-2006_03
ORD IDord-d7c675b9ee8e41cd9e3d5f36d3576b26
Source noteuspto-grants-2006_03