HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 5-Methoxy-6-methylindoline-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-hydroxyimino-N-(4-methoxy-3-methylphenyl)acetamide | HCID 71334693 | — |
| Product | 5-Methoxy-6-methylindoline-2,3-dione | HCID 54329184 | 77% |
Reaction Steps
2-Hydroxyimino-N-(4-methoxy-3-methylphenyl)acetamide (0.5 g, 2.4 mmol) was added portionwise to concentrated methanesulfonic acid (1.5 mL). The 2-hydroxyimino-N-(4-methoxy-3-methylphenyl)acetamide was added over a period of 45 min in order to keep the reaction temperature between 65 to 70° C. After addition, the mixture was stirred for 10 min and then poured onto ice (10 g). The resulting aqueous solution was extracted with ethyl acetate (3×50 mL). Combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by column chromatography on silica gel with petroleum ether:ethyl acetate (20:1, v/v) as eluent to afford 5-methoxy-6-methyl-1H-indole-2,3-dione (350 mg, 1.8 mmol, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807686B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-d21d2f10338542aaafa2cfd338b1d777 |
| Source note | uspto-grants-2010_10 |