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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325914Generated: October 30, 2026

Sodium Hydroxide → 5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)-pyrimidinone

https://huagongshe.com/reaction/325914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Chloro-2-butanoneHCID 20026—
ReactantSodium BicarbonateHCID 516892—
ReactantN,N,N-triethylbenzeneethanaminium chlorideHCID 20262408—
ReactantHCID 178433550HCID 178433550—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)-pyrimidinoneHCID 135674650—

Reaction Steps

A mixture of 30 parts of 4-hydroxy-2-mercapto-6-methyl-5-pyrimidineethanol, 6.8 parts of sodium hydroxide, 15 parts of sodium hydrogen carbonate and 100 parts of 2-propanone was stirred at room temperature and there were added 180 parts of tetrahydrofuran and 170 parts of water. Then there were added at once 25 parts of 3-chloro-2-butanone and 0.2 parts of N,N,N-triethylbenzeneethanaminium chloride and the whole was stirred and heated for 1 hour at 60° C. Stirring was continued overnight at room temperature. The reaction mixture was filtered and the filtrate was salted out. The organic phase was separated, dried, filtered and evaporated, yielding 36 parts of 5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)-pyrimidinone as an oily residue (intermediate 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443451
Source datasetuspto-grants-1984_04
ORD IDord-6e4ecfd2bff14e5cb9b1b0c73aa99639
Source noteuspto-grants-1984_04