HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334878Generated: October 25, 2026
Benzyl Bromide → Methyl 5-acetyl-2,4-bis-benzyloxybenzoate
https://huagongshe.com/reaction/334878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-acetyl-2,4-dihydroxybenzoate | HCID 12482079 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-acetyl-2,4-bis-benzyloxybenzoate | HCID 11955869 | 142.8% |
Reaction Steps
Methyl 5-acetyl-2,4-dihydroxybenzoate (2.62 g, 12.48 mmol) was dissolved in acetonitrile (40 ml), anhydrous potassium carbonate (4.93 g, 35.7 mmol) was added and the stirred mixture was treated with benzyl bromide (5.09 g, 29.75 mmol) and held at reflux for 3 hours. Upon cooling the solvent was removed in vacuo and the mixture partitioned between water and dichloromethane. The organic layer was separated and the solvent removed in vacuo to afford methyl 5-acetyl-2,4-bis-benzyloxybenzoate (3.48 g, 71%) as a colourless solid which was dried at 50° C. in a vacuum oven and used without further purification. 1H NMR (DMSO-d6) 8.21 (1H, s), 7.55 (4H, m), 7.43 (4H, m), 7.37 (2H, m), 7.04 (1H, s), 5.38 (4H, s), 3.79 (3H, s), 2.48 (3H, s). MS: [M+H]+ 391.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883790B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-fb055f8b97524905850963d1066ad371 |
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| Source note | uspto-grants-2014_11 |
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