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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485643Generated: October 28, 2026

Ethanol → 5-benzyl-6-methyl-2-methylsulfanyl-1H-pyrimidin-4-one

https://huagongshe.com/reaction/485643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant5-Benzyl-6-methylthiouracilHCID 697326—
SolventWaterHCID 962—
Product5-benzyl-6-methyl-2-methylsulfanyl-1H-pyrimidin-4-oneHCID 135422583—

Reaction Conditions

Temperature60 °C

Reaction Steps

5-Benzyl-6-methylthiouracil (6.0 gms) and sodium hydroxide (1.06 gms) were dissolved in water (30 mls). The solution was cooled and ethanol (60 mls) and methyl iodide (3.67 gms) added with stirring. The mixture was heated at 60° C. for 1/2 hour, cooled and the resulting solid collected and water-washed. A second crop of solid was obtained by acidification of the filtrate to pH=4 with acetic acid. Recrystallisation from ethanol produced 5-benzyl-6-methyl-2-methylthio-4-pyrimidone (5.53 gms) m.p.=220°-221.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537779
Source datasetuspto-grants-1985_08
ORD IDord-742c98ff561348c380b4bd890f855b6e
Source noteuspto-grants-1985_08