HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 1,3-Dihydro-5-methoxy-1-methyl-2H-indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methoxyoxindole | HCID 1514286 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Dihydro-5-methoxy-1-methyl-2H-indol-2-one | HCID 9102194 | 53.1% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A dry round-bottom flask was charged with NaH (60% wt) (64 mg, 1.61 mmol) and toluene (2.0 mL). The suspension was heated to 100° C. and then 5-methoxyindolin-2-one (250 mg, 1.53 mmol) was added. After 30 min at 100° C. Me2SO4 (0.16 mL, 1.68 mmol) was added and the temperature maintained at 100° C. for 2.5 h. The reaction was cooled to room temperature and the solvent removed. The residue was purified by column chromatography (silica gel, 25-33% EtOAc in hexane) to give 5-methoxy-1-methylindolin-2-one (beige solid, 144 mg, 53%); MS ESI 164.1 [M+H]+, calcd for [C9H9NO2+H]+ 164.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921545B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-860679f21e074b1bbd4dffe93a2f1652 |
| Source note | uspto-grants-2014_12 |