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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166607Generated: October 29, 2026

Benzoyl chloride → 1-(2'-O-Benzoyl-beta-D-ribopyranosyl)-5-(2-phtalimidoethyl)uracil

https://huagongshe.com/reaction/1166607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-(2-Phtalimidoethyl)-1-(beta-D-ribopyranosyl)uracilHCID 15408030—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product1-(2'-O-Benzoyl-beta-D-ribopyranosyl)-5-(2-phtalimidoethyl)uracilHCID 1540803160,597.301%

Reaction Conditions

Temperature-70 °C

Reaction Steps

10.6 g (0.025 mmol) of 5-(2-phtalimidoethyl)-1-(β-D-ribopyranosyl)uracil were dissolved in 20 ml of pyridine in a heated and argon-flushed 1 l four-necked flask and mixed with 200 ml of dichloromethane. The mixture was cooled to −70° C., 3.82 ml (0.033 mmol) of benzoyl chloride in 5 ml of pyridine and 20 ml of dichloromethane were slowly added dropwise with cooling and the mixture was stirred at −70° C. for 35 min. The reaction mixture was poured onto 600 ml of cooled ammonium chloride solution and the aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with water, dried and concentrated to dryness in vacuo. Chromatography on silica gel (ethyl acetate/heptane 1:1) yielded 7.9 g (60%) of 1-(2′-O-benzoyl-β-D-ribopyranosyl)-5-(2-phtalimidoethyl)uracil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613894B1
Source datasetuspto-grants-2003_09
ORD IDord-4fc8a1c354af4d26ae84142fd43279de
Source noteuspto-grants-2003_09