HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Methyl 3-methoxy-5-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 3-Hydroxy-5-methylbenzoic acid | HCID 231756 | — |
| Product | Methyl 3-methoxy-5-methylbenzoate | HCID 13834966 | 93.5% |
Reaction Steps
To acetone (180 mL) were added 3-hydroxy-5-methylbenzoic acid (9 g, 59.16 mmol), potassium carbonate (33 g, 237 mmol) and methyl iodide (37.2 mL, 591.6 mmol). For O-methylation, the resulting mixture was heated at 65° C. for 12 hours in the presence of a catalytic amount of dimethylaminopyridine. After vacuum distillation of the acetone, the concentrate was treated in water (300 mL) and dichloromethane (450 mL). The organic layer was dried over anhydrous magnesium sulfate and subjected to distillation. Column chromatography (silica gel, ethyl acetate-hexane 1:12 v/v) with the residue produced the title compound as a colorless liquid (9.98 g, 93.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273880B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-4943c0aa57844adf823ef184858acff4 |
| Source note | uspto-grants-2012_09 |