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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516772Generated: November 3, 2026

Vinyl Acetate → 1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracil

https://huagongshe.com/reaction/1516772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
ReactantTriphenylphosphineHCID 11776—
ReactantCalcium HydroxideHCID 6093208—
Reactant1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-iodouracilHCID 57838982—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracilHCID 10037283475.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of palladium (II) acetate (79 mg, 0.35 mmol), triphenylphosphine (185 mg, 0.7 mmol) and triethylamine (5 ml), (dried over calcium hydroxide) in dry DMF (80 ml) was maintained at 70° C. with stirring until an intense red color appeared. Compound 19 (2.36 gm, 6.95 mmol) and vinyl acetate (30 ml, 330 mmol) were then added, and the reaction was allowed to proceed at 70° C. for 6 h with stirring. The solvent was removed in vacuo and the residue obtained was extracted with water (2×50 ml). The water layer was washed with dichloromethane, evaporated in vacuo, and the residue obtained was purified by elution from a silica gel column using ethyl acetate-methanol (95:5, v/v) as eluent to give 20 as a viscous oil (800 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227594B2
Source datasetuspto-grants-2012_07
ORD IDord-bcadf2594cd346e8baa5b1374bea1ba2
Source noteuspto-grants-2012_07