Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516775Generated: November 4, 2026

Benzoyl chloride → 1-[4-Benzoyloxy-3-(benzoyloxymethyl)-1-butyl]-5-vinyluracil

https://huagongshe.com/reaction/1516775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracilHCID 10037283—
SolventPyridineHCID 1049—
Product1-[4-Benzoyloxy-3-(benzoyloxymethyl)-1-butyl]-5-vinyluracilHCID 1109158465.6%

Reaction Steps

Benzoylchloride (600 mg, 4.2 mmol) was added to a solution of 20 (450 mg, 1.87 mmol) in dry pyridine (50 ml) and the reaction was allowed to proceed at 25° C. with stirring for 48 h. The reaction mixture was poured onto ice water (50 ml) and extracted with dichloromethane (3×50 ml). The dichloromethane extract was dried over sodium sulfate, the solvent was removed in vacuo and the residue obtained was purified by elution from a silica gel column using chloroform-methanol (97:3, v/v) as eluent to yield 22 as a viscous oil (550 mg, 65.4%) which was used directly in the next reaction step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227594B2
Source datasetuspto-grants-2012_07
ORD IDord-bec846b79aba47239aba663ba4bcce8b
Source noteuspto-grants-2012_07