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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860843Generated: October 31, 2026

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

https://huagongshe.com/reaction/860843

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 numberUS07153955B2
Source datasetuspto-grants-2006_12
ORD IDord-5a9a8a470c4f4e4682d84ef7255904f2
Source noteuspto-grants-2006_12