HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19921676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 5-Cyanogramine | HCID 33033 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19921676 | HCID 19921676 | 96% |
Reaction Steps
To a solution of 2.7 g (13.6 mmol, 1.0 equiv.) of 5-cyano-3-(dimethylamino)methyl-1H-indole in 125 mL of THF at 0° C. was added 1.3 mL (20.3 mmol, 1.5 equiv.) of methyl iodide dropwise. After five minutes the solution was allowed to warm to room temperature and stirred for one hour. The resulting precipitate was filtered and dried in vacuo to yield 4.4 g (96%) of N,N,N-trimethyl-1-(5-cyano-1H-indol-3-yl)methanaminium iodide, pure by 1H NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434154 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-c146cf92b90048c98395a6c5c59099f9 |
| Source note | uspto-grants-1995_07 |