HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 72943024, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Hydroxy-6-methyl-2H-1-benzopyran-2-one | HCID 54686349 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 72943024 | HCID 72943024 | 43.3% |
Reaction Steps
To a solution of 4-hydroxy-6-methylcoumarin (300 mg, 1.70 mmol) in 3.4 mL of dry N,N-dimethylformamide was added sodium hydride (89 mg, 55%, 2.0 mmol) under nitrogen at 0° C. After the reaction mixture was stirred at room temperature for 30 min, methyl iodide (0.16 mL, 2.6 mmol) was added with additional stirring for 30 min. The reaction mixture was diluted with 10 mL of ethyl acetate and 10 mL of saturated NH4Cl aqueous solution at 0° C., successively, and the solution was extracted with 100 mL of ethyl acetate. The extract was washed with saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the solution was concentrated in vacuo to obtain crude 4-methoxy-6-methylcoumarin (140 mg, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962674B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-4cb0b21e58ef44d196ba86d8917ed82c |
| Source note | uspto-grants-2015_02 |