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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Methyl (methylthio)acetate | HCID 85522 | — |
| Reactant | Proton sponge | HCID 88675 | — |
| Reactant | 4-Methoxy-2,3-dimethylaniline | HCID 11094809 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6,7-Dimethyl-5-methoxy-3-(methylthio)-1,3-dihydro-2H-indole-2-one | HCID 22238077 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07008940B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-d7c675b9ee8e41cd9e3d5f36d3576b26 |
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| Source note | uspto-grants-2006_03 |
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