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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466085Generated: October 26, 2026

Benzene → Uridine, 2'-deoxy-5-fluoro-3'-O-(phenylmethyl)-

https://huagongshe.com/reaction/466085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
Reactant2'-deoxy-5'-O-trityl-5-fluorouridineHCID 10838704—
Solvent1,4-DioxaneHCID 31275—
ProductUridine, 2'-deoxy-5-fluoro-3'-O-(phenylmethyl)-HCID 1066457420%

Reaction Steps

To a mixture of 50 ml of benzene and 50 ml of dioxane were added 1.00 g of 2'-deoxy-5-fluoro-5'-O-trityluridine, 0.30 ml of benzyl bromide and 0.23 g of potassium hydroxide powder, and the mixture was refluxed for 25 hours. The insolubles were removed by filtration and the filtrate was concentrated and the concentrate was dissolved in 5 ml of 80% acetic acid. The solution was left to stand at 80° C. for 2 hours. The solvent was distilled off and the residue was placed on a silica gel column to conduct a gradient elution using chloroform and mixtures of methanol (up to 2%) and chloroform. The fractions corresponding to 3'-O-benzyl-2'-deoxy-5-fluorouridine were collected and concentrated. The concentrate was recrystallized from ethanol, giving 0.14 g of the title compound in a yield of 20%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155113
Source datasetuspto-grants-1992_10
ORD IDord-85b329a2a10f4a8388d5b30f839bd77c
Source noteuspto-grants-1992_10