HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623623Generated: October 31, 2026
5-Bromosalicylic acid → Benzyl 2-(benzyloxy)-5-bromobenzoate
https://huagongshe.com/reaction/1623623
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
(Bromomethyl)benzene (34.2 ml, 288 mmol) was added over 5 minutes to a stirred suspension of 5-bromo-2-hydroxybenzoic acid (28.4 g, 131 mmol) and potassium carbonate (45.2 g, 327 mmol) in acetone (300 ml) in air at room temperature. The reaction mixture was stirred at 70° C. overnight. After filtering, the filtrate was evaporated to give a light yellow oil, dried in a vacuum to give yellow solid, which was washed by petroleum ether (300 ml×2), filtered and dried in vacuum to yield the title compound as a white solid. 48.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778939B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-6429c0d3bcca474fb681ab40febefc17 |
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| Source note | uspto-grants-2014_07 |
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