HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 54508469, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | sodium 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioate | HCID 23695420 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54508469 | HCID 54508469 | — |
Reaction Steps
A solution of sodium 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioate (3 g, prepared in the previous Example) and methyl iodide (0.5 ml) in 95% ethanol (15 ml) is refluxed for one hour. The orange reaction mixture is concentrated, taken up with ether and washed with water. The organic phase is dried over sodium sulfate and concentrated. After chromatography on silica gel (eluent: cyclohexane/AcOEt 70/30), methyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carbodithioate (13 g) is obtained in the form of an oil, which is taken up with pentene to give a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05418242 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-4a8537d9c43449d3a739c166cafcbc0e |
| Source note | uspto-grants-1995_05 |