HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Methoxy-5-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-5-nitrobenzonitrile | HCID 11116377 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Methoxy-5-nitrobenzonitrile | HCID 82677 | — |
Reaction Steps
A mixture of 2-cyano-4-nitrophenol (3.5 g, 21 mmol), K2CO3 (5.9 g, 42 mmol), and MeI (9.08 g, 64 mmol) in acetone (50 mL) was heated at reflux overnight. The mixture was cooled and concentrated, taken up in H2O, stirred, filtered the yellow solid, dried by air (3.0 g, 79%). 1H NMR (400 MHz, CDCl3): d 4.08 (s, 3H), 7.12 (d, J=9.2 Hz, 1H), 8.5 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294531B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-c383916518ed4d8980d5fe45527822a9 |
| Source note | uspto-grants-2001_09 |