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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-AcetyluracilHCID 234581—
SolventDimethylformamideHCID 6228—
Product5-Acetyl-1,3-dibenzyluracilHCID 1167440879.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569573B2
Source datasetuspto-grants-2009_08
ORD IDord-b63df88513e4478988819180560472a1
Source noteuspto-grants-2009_08