HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Methyl-6-(methylthio)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-(Methylsulfanyl)-1H-indole | HCID 19848917 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methyl-6-(methylthio)-1H-indole | HCID 53996658 | 91% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 6-methylsulfanyl-1H-indole (6.8 g, 42 mmol) in DMF (50 mL) was added to a slurry of NaH (55 mmol) in DMF(10 mL) at 0° C. over a period of 10 minutes. After stirring for 1 hour at 0° C., CH3I (4.0 ml,64 mmol) was added and the mixture stirred for 30 minutes at 0° C., then at room temperature for 1 hour, then poured into ice/H2O and extracted with EtOAc. The organic phase was washed with saturated NaCl solution, dried over MgSO4, filtered and evaporated to give 6.7 g (91.0%) of 1-methyl-6-methylsulfanyl-1H-indole as a yellow oil after flash column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891901 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-08e88a35d97e4956842d2a7a999c2e64 |
| Source note | uspto-grants-1999_04 |