HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 3-(benzyloxy)-5-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-(benzyloxy)-5-hydroxybenzoate | HCID 7472028 | 34% |
Reaction Steps
A mixture of 8.40 g (0.05 mmol) methyl 3,5-dihydroxybenzoate (159) and 7.60 g (0.055 mmol) of potassium carbonate in 250 mL of acetone was stirred at room temperature for 30 min. Then 8.55 g (0.05 mmol) of benzyl bromide dissolved in 100 mL of acetone was added. The suspension was refluxed for 24 h. The solid was filtered, and the filtrate was evaporated. The residue was purified by column chromatography (SiO2, CH2Cl2/EtOAc=9/1) to give 160.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524740B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-84eaaa2eaa734cbb920c9edc10073735 |
| Source note | uspto-grants-2013_09 |