HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-[2,3-Dihydro-5-(methylthio)-1H-indol-1-yl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10535785 | HCID 10535785 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2,3-Dihydro-5-(methylthio)-1H-indol-1-yl]ethanone | HCID 10655946 | 93.2% |
Reaction Steps
A mixture of 1-acetyl-5-mercaptoindoline (D3) (0.98 g, 5.07 mmol), methyl iodide (0.35 ml, 5.6 mmol) and triethylamine (0.78 ml, 5.6 mmol) in dichloromethane (25 ml) was stirred for 18 h at room temperature. The mixture was evaporated, and the residue was redissolved in dichloromethane and washed with dilute hydrochloric acid. The organic solution was dried and evaporated to give the title compound (0.98 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834494 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-bafeccf7209a4234b63c6054434ab550 |
| Source note | uspto-grants-1998_11 |