HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 3-(benzyloxy)-5-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-(benzyloxy)-5-hydroxybenzoate | HCID 7472028 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-(benzyloxy)-5-methoxybenzoate | HCID 12658782 | 85% |
Reaction Steps
A suspension of 4.0 g (0.0165 mmol) methyl 3-(benzyloxy)-5-hydroxybenzoate (160), 6.84 g (0.0495 mmol) potassium carbonate, and 11.71 g (0.0825 mmol) iodomethane in the 200 mL of acetone was stirred at room temperature for 24 h. After the mixture was filtered and evaporated, the residue was washed with water. The methyl 3-(benzyloxy)-5-methoxybenzoate (161) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524740B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-34cdac811085477c8b89e990af9512d2 |
| Source note | uspto-grants-2013_09 |