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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728204Generated: October 31, 2026

p-Anisoyl chloride → HCID 53936791, compound

https://huagongshe.com/reaction/728204

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantHCID 18646879HCID 18646879—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53936791HCID 5393679191.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 0.30 g of 5'-O-acetyl-2'-deoxy-5-fluoro-3'-O-(2-thienyl)methyluridine in 10 ml of dioxane were added 0.55 ml of triethylamine and 0.16 g of 4-methoxy-benzoyl chloride. The mixture was stirred at 80° C. for 2 hours. The solvent was distilled off and the residue was dissolved in 30 ml of ethyl acetate. The solution was washed with water. The ethyl acetate layer was dried over sodium anhydrous sulfate and concentrated. The residue was subjected to silica gel chromatography and purified by elution with chloroform, giving 0.37 g of 5'-O-acetyl-2'-deoxy-5-fluoro-3-(4-methoxybenzoyl)-3'-O-(2-thienyl)me thyluridine in a yield of 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047521
Source datasetuspto-grants-1991_09
ORD IDord-4c2a669e7f30480b8bdb0e783962982f
Source noteuspto-grants-1991_09