HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 3-cyano-4-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-cyano-4-hydroxybenzoate | HCID 11769089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-cyano-4-methoxybenzoate | HCID 2801011 | — |
Reaction Steps
3-cyano-4-hydroxybenzoic acid methyl ester from step 1 (1 g, 3.6 mmol) was dissolved in DMF (18 ml) and treated with NaH (290 g, 7.2 mmol) and CH3I (450 μl, 7.2 mmol). The reaction mixture was stirred at room temperature for 24 hours. EtOAc was added to the mixture and extracted with 5% citric acid (2×10 mL), saturated NaHCO3 (2×10 mL) and brine (1×10 mL). The organic layer was dried (MgSO4), filtered, and concentrated to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06077853 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-24d5702524d44c468ed6dff94ce807df |
| Source note | uspto-grants-2000_06 |