HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → N-Methyl-N-(5-nitrobenzofur-2-ylmethyl)-4-nitrophenethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-4-nitrophenethylamine | HCID 2794239 | — |
| Reactant | 2-(Bromomethyl)-5-nitro-1-benzofuran | HCID 11414179 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-Methyl-N-(5-nitrobenzofur-2-ylmethyl)-4-nitrophenethylamine | HCID 15735404 | — |
Reaction Steps
N-Methyl-4-nitrophenethylamine (0.41 g, 2.3 mmole), 2-bromomethyl-5-nitrobenzofuran (0.66 g, 2.6 mmole), sodium iodide (0.39 g, 2.6 mmole) and potassium carbonate (0.36 g, 2.6 mmole) were heated at reflux temperature in acetonitrile (50 ml) for 8 days. The solvent was then evaporated, water was added, and the mixture extracted three times with methylene chloride. The combined organic extracts were washed with water, dried (MgSO4) and evaporated to give a semi-solid which was recrystallised from isopropanol to give the title compound, yield 380 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04956382 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-fd4b4e5e7b8f427cb8ca55d75d70f224 |
| Source note | uspto-grants-1990_09 |