HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099237Generated: October 30, 2026
Benzyl Bromide → 5-Acetyl-1,3-dibenzyluracil
https://huagongshe.com/reaction/2099237
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Acetyluracil | HCID 234581 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Acetyl-1,3-dibenzyluracil | HCID 11674408 | 79.9% |
Reaction Steps
A suspension of 5-acetyluracil (3.1 g, 20 mmol), and potassium carbonate (6.9 g, 50 mmol) in DMF (75 ml) was stirred for 20 min. Then benzyl bromide (6.0 ml, 50 mmol) was added. The resulting mixture was stirred for 8 h at room temperature. DMF was distilled under vacuum. The residue was purified by column (dichloromethane:methanol 40:1). The appropriate fraction was concentrated and crystallized from ethanol to afford 5.34 g of a white solid. Yield was 79.8%. Mp. 92-93° C. 1HNMR (CDCl3): 8.23 (s, 1H), 7.29-7.49 (m, 10H), 5.17 (s, 2H), 5.01 (s, 2H), 2.62 (s, 3H). 13CNMR (CDCl3): 194.5, 160.7, 151.0, 148.4, 136.2, 134.4, 129.2, 129.0, 128.9, 128.5, 128.2, 127.8, 112.2, 53.4, 44.9, 30.7. FAB-HRMS: [M+H]+ Calcd. for C20H19N2O3 335.1396. Found 335.1412.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569573B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b63df88513e4478988819180560472a1 |
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| Source note | uspto-grants-2009_08 |
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