HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 5-methoxy-1-methyl-3-(methylthio)-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 5-methoxy-3-(methylthio)-1H-indole-2-carboxylate | HCID 10538712 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-methoxy-1-methyl-3-(methylthio)-1H-indole-2-carboxylate | HCID 10730410 | 88% |
Reaction Steps
A suspension of 60% sodium hydride in mineral oil (0.30 g, 7.5 mmol) in 3.0 mL of N,N-dimethylformamide is cooled in ice while a solution of methyl 5-methoxy-3-(methylthio)-1H-indole-2-carboxylate (1.3 g, 5.2 mmol) in 10 mL of N,N-dimethylformamide is added dropwise. The mixture is stirred for 45 minutes, then iodomethane (0.50 mL, 1.1 g, 8.0 mmol) is added in one portion. After stirring at room temperature for 8 hours, the mixture is added to 100 g of ice and water. The solid is filtered and washed with 10% methanol-water to yield 1.2 g (88%) of product. A sample purified by flash chromatography (silica gel, 25% hexane in dichloromethane elution) and recrystallized from hexane has mp 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424329 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-03311f3de5584e87aa4d6b82483962f2 |
| Source note | uspto-grants-1995_06 |