HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Methyl-7-nitro-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Nitro-1,2,3,4-tetrahydroquinoline | HCID 252513 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methyl-7-nitro-1,2,3,4-tetrahydroquinoline | HCID 11480955 | — |
Reaction Steps
To a solution of the 7-nitro-1,2,3,4-tetrahydroquinoline (4.5 g, 25.25 mmol) in DMF (50 mL) was added potassium carbonate (15 g) followed by iodomethane (5.54 g, 39.0 mMol) and the mixture was agitated overnight at ambient temperature. The mixture was poured onto water and extracted with ether (3×200 mL). The combined ethereal extracts were washed with brine, dried and concentrated to give the crude product which was purified by column chromatography on silica-gel to obtain the title compound as an orange liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312233B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-55631c51fe0445dd835efdad689fbc46 |
| Source note | uspto-grants-2007_12 |