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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746254Generated: October 30, 2026

Potassium Iodide → 6-Chloro-1-butyl-3-propyluracil

https://huagongshe.com/reaction/746254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantButyl bromideHCID 8002—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-3-propylpyrimidine-2,4(1H,3H)-dioneHCID 640846—
SolventDimethylformamideHCID 6228—
Product6-Chloro-1-butyl-3-propyluracilHCID 23310765—

Reaction Steps

A mixture of 7 g of 6-chloro-3-propyluracil, 10.28 g of butyl bromide, 10.28 g of potassium carbonate, 6 g of potassium iodide and 80 ml of dimethylformamide was stirred at room temperature for 23 hours. After the reaction solution was concentrated to dryness under reduced pressure, 300 ml each of chloroform and water were added to the residue, and the mixture was shaken. The chloroform layer was washed with water and then concentrated to dryness under reduced pressure to give 6-chloro-1-butyl-3-propyluracil as a brown oily substance. This product, without being purified, was dissolved in 20 ml of ethanol, and 20 ml of 100% hydrazine hydrate was added to the solution, followed by stirring at room temperature for 1 hour. The reaction solution was concentrated to dryness under reduced pressure and the residue was washed with water and recrystallized from a mixture of ethanol, ethyl acetate and isopropyl ether to give 7 g of yellow prisms of 6-hydrazino-1-butyl-3-propyluracil melting at 146°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603203
Source datasetuspto-grants-1986_07
ORD IDord-2b00b6cd262b48e9853abae1963e8b52
Source noteuspto-grants-1986_07