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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607339Generated: November 4, 2026

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

https://huagongshe.com/reaction/1607339

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 numberUS04864021
Source datasetuspto-grants-1989_09
ORD IDord-8423f983e7ef4094bd84d8d5f9d63374
Source noteuspto-grants-1989_09