HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424047Generated: October 26, 2026
Acetone → Benzyl-2,4-bis-benzyloxy-5-bromobenzoate
https://huagongshe.com/reaction/424047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-2,4-dihydroxybenzoic acid | HCID 81814 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl-2,4-bis-benzyloxy-5-bromobenzoate | HCID 46915635 | — |
Reaction Steps
To a 10 L jacketed vessel, fitted with a flange lid containing stirrer, thermometer and dropping funnel, was charged acetone (2.5 L) followed by 5-bromo-2,4-dihydroxybenzoic acid (100 g, 0.43 mol) and potassium carbonate (356 g, 2.58 mol). To the stirring mixture at ambient was added benzyl bromide (185 mL, 1.55 mol) at a rate of 20 ml/min. The mixture was heated at 60° C. for 18 h and then taken to 45° C. Water (1.5 L) was added and the mixture stirred for 30 min. The mixture was extracted with EtOAc (2×1 L) and the combined organic portions reduced in vacuo. To the residue was added Et2O (200 mL) and petroleum ether (1 L), the mixture stirred for 30 min and the solid formed collected by filtration and dried in vacuo to give the title compound (1 97.2 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101648B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c956d5cefe9c4af7bbe0c8fdf973b62c |
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| Source note | uspto-grants-2012_01 |
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