HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(2-Methoxy-5-nitrobenzyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 86760686 | HCID 86760686 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-Methoxy-5-nitrobenzyl)acetamide | HCID 20650534 | — |
Reaction Steps
N-(2-Methoxy-5-nitrobenzyl)acetamide 2-Acetamidomethyl-4-nitrophenol (2 g), sodium carbonate (2 g) and iodomethane (2 ml) were stirred in acetone (30 ml) at reflux 4 h. The mixture was filtered, the filtrate evaporated to dryness. The residue was warmed with aqueous sodium carbonate, washed with water and dried. Crystallised from ethanol/dilute acetic acid to give N-(2-methoxy-5-nitrobenzyl)acetamide as buff prisms. MP: 158.5-159.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384963B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-90d9c20ccdbb45d28f3a8b946592ef38 |
| Source note | uspto-grants-2008_06 |