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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380232Generated: November 3, 2026

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

https://huagongshe.com/reaction/1380232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Chloro-2-butanoneHCID 20026—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178433550HCID 178433550—
CatalystBenzyl triethylammonium chlorideHCID 66133—
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-triethylbenzenemethanaminium 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 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581171
Source datasetuspto-grants-1986_04
ORD IDord-fe257c747dc941458fa5fb0bfe3b26c2
Source noteuspto-grants-1986_04