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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250988Generated: November 3, 2026

Water → 6-(1fluoroethyl)-4-pyrimidone

https://huagongshe.com/reaction/1250988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantFormamidine acetateHCID 160693—
ReactantMethyl 4-fluoro-3-oxopentanoateHCID 9793838—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product6-(1fluoroethyl)-4-pyrimidoneHCID 13547180789.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution in which 9.33 g of methyl 4-fluoro-3-oxopentanoate had been dissolved in 115 ml of methanol were successively added 36.5 g of a 28% sodium methoxide methanol solution and 9.84 g of formamidine acetate at room temperature, and the mixture was stirred at 40° C. for 12 hours. To the mixture was further added 0.66 g of formamidine acetate and after stirring the mixture at 50° C. for 2 hours, the mixture was cooled to 10° C. or lower. After cooling, a mixture of 9.51 g of conc. sulfuric acid and 8.5 g of water was added to the reaction mixture. After stirring the mixture at 50° C. for 30 minutes, insolubles were removed by filtration and the filtrate was quantitated by the liquid chromatography internal standard method. As a result, 7.99 g of 6-(1-fluoroethyl)-4-pyrimidone was found to be formed (yield: 89.2%). The filtrate was concentrated under reduced pressure and the concentrated solution was recrystallized from 40 ml of 2-propanol to obtain 5.82 g of 6-(1-fluoroethyl)-4-pyrimidone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340757B1
Source datasetuspto-grants-2002_01
ORD IDord-57b9d174bb9948fbae194e1e957d15b2
Source noteuspto-grants-2002_01