HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332657Generated: October 25, 2026
Benzyl Bromide → Benzyl 3-bromo-5-hydroxybenzoate
https://huagongshe.com/reaction/332657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-5-hydroxybenzoic acid | HCID 15735511 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 3-bromo-5-hydroxybenzoate | HCID 71093147 | 100.6% |
Reaction Steps
To a stirred solution of 3-bromo-5-hydroxybenzoic acid (2 g, 9.22 mmol) in dimethyl formamide (50 mL), was added potassium carbonate (1.27 g, 9.21 mmol), and the mixture was stirred at 0° C. for 20 minutes. Benzyl bromide (1.1 mL, 9.25 mmol) was added, and the reaction mixture allowed to warm to room temperature over 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (×3). The combined organic extracts were washed with brine, dried (magnesium sulphate), filtered, and concentrated under reduced pressure to afford the title compound (2.85 g, quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877774B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-b84a3e732df34143b7f55f33667b13c4 |
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| Source note | uspto-grants-2014_11 |
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