HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-methoxy-3-methylsulfanyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-methoxy-3-thiocyanato-1H-indole | HCID 22574114 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-methoxy-3-methylsulfanyl-1H-indole | HCID 22574077 | 37.9% |
Reaction Steps
To a solution of 6-methoxy-3-thiocyanato-1H-indole (0.336 g, 1.64 mmole) and methyl iodide (0.700 g, 4.93 mmole) in methanol (10 ml) was added potassium hydroxide solution (0.164 ml, 10N) at 0° C. The reaction mixture was stirred for 1 h at room temperature. Silica gel (5 g) was added to the reaction mixture and the solvent was removed under reduced pressure. The residue was purified on a column of silica gel, eluting the product with mixtures of ethyl acetate:hexane (1:9 to 1:1). The first product which was eluted was the desired 6-methoxy-3-methylsulfanyl-1H-indole (0.120 g, 37% yield) followed by 6-methoxy-1H-indole-3-thiol (0.126 g). Step 3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852726B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-c6e4ec08a77f4c4ebf36a51163d07893 |
| Source note | uspto-grants-2005_02 |