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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703560Generated: October 30, 2026

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

https://huagongshe.com/reaction/703560

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 numberUS04983609
Source datasetuspto-grants-1991_01
ORD IDord-d96685647abd4802b78145b91fac0fc4
Source noteuspto-grants-1991_01