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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980180Generated: October 26, 2026

5-Chloro-2(1H)-pyrimidinone → 5-Chloro-1-(4-methylsulphinylphenacyl)pyrimidin-2-one

https://huagongshe.com/reaction/980180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
Reactant4-Methylsulphinylphenacyl bromideHCID 12795537—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
Product5-Chloro-1-(4-methylsulphinylphenacyl)pyrimidin-2-oneHCID 1279554654.6%

Reaction Steps

A suspension of 5-chloropyrimidin-2-one (399 mg). and 2-bromo-4'-methylsulphinylacetophenone (784 mg) in triethylamine (1 ml) and ethanol (20 ml) was stirred at ambient temperature for one hour, when the resulting suspension was chilled in ice. The collected solid was crystallised from ethanol to give the title pyrimidinone (509 mg,); m.p. 219°-220°; λmaxEtOH 233.5 nm (ε 17920), 332 nm (ε 2060), λinf 266 nm (ε 9280).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636509
Source datasetuspto-grants-1987_01
ORD IDord-f6f43282221c4ea9a03bb8905fb42953
Source noteuspto-grants-1987_01