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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466104Generated: October 25, 2026

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

https://huagongshe.com/reaction/466104

Reaction equation

Participants

RoleNameHCIDCharge
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 1066457472.6%

Reaction Steps

In 50 ml of dioxane was dissolved 10 g of 2'-deoxy-5'-O-trityl-5-fluorouridine. To the solution were added 2.9 ml of benzyl bromide and 14.6 g of particles of potassium hydroxide. The mixture was stirred at room temperature for 1 hour. The solvent was distilled off and the residue was dissolved in 80 ml of a 80% solution of acetic acid to undergo reaction at 50° to 60° C. for 2 hours. The reaction mixture was cooled with ice for 1 hour, the trityl alcohol was separated by filtration and the mother liquor was concentrated. To the concentrate was added ethanol and the mixture was stirred. The crystals precipitated were separated by filtration and dried, affording 5.0 g of the title compound in a yield of 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155113
Source datasetuspto-grants-1992_10
ORD IDord-70939b8e63cd4aa28cc987d78df48095
Source noteuspto-grants-1992_10