HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromosalicylic acid → Benzyl 2-(benzyloxy)-5-bromobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromosalicylic acid | HCID 6972 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Benzyl 2-(benzyloxy)-5-bromobenzoate | HCID 17750009 | — |
Reaction Steps
Neat (bromomethyl)benzene (17.10 g, 100 mmol) was added to a stirred suspension of 5-bromo-2-hydroxybenzoic acid (8.68 g, 40.0 mmol) and potassium carbonate (13.82 g, 100 mmol) in acetone (150 ml) at 20° C. over 1 min. The reaction mixture was refluxed overnight. After filtration, the filtrate was evaporated to yield the title compound as an oil which was used in the next step without further purification. 15 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778939B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-d613d9520afd4a8c88d8692ad46c142b |
| Source note | uspto-grants-2014_07 |