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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759565Generated: October 30, 2026

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

https://huagongshe.com/reaction/1759565

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 numberUS04341787
Source datasetuspto-grants-1982_07
ORD IDord-fa0b220473e54f4db899d8a337de9858
Source noteuspto-grants-1982_07