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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434659Generated: October 31, 2026

5-Chloro-2(1H)-pyrimidinone → HCID 20491782, compound

https://huagongshe.com/reaction/434659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
ReactantSodium BicarbonateHCID 516892—
Reactant2(3H)-Furanone, dihydro-4-methylene-HCID 12303360—
SolventEthanolHCID 702—
ProductHCID 20491782HCID 2049178224%

Reaction Steps

A suspension of 5-chloropyrimidin-2-one (1.007 g) and sodium hydrogen carbonate (647 mg) in 3-methylene-γ-butyrolactone (1.208 g) and ethanol (50 ml) was stirred and heated at reflux. After 2 h, the suspension was cooled and filtered. The filtrate was evaporated and the residue and solid were combined and boiled in ethyl acetate (150 ml). The resulting suspension was filtered and the filtrate evaporated to a pale cream solid. The solid from the filtration was treated with water (50 ml) and the resulting suspension filtered to give a solid which was combined with the pale cream solid and recrystallised from methanol to give white crystals of the title pyrimidinone (424 mg), m.p. 283°-284° C., λmax (EtOH) 229.5 nm (ε 7,700), 332 nm (ε 2,100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399140
Source datasetuspto-grants-1983_08
ORD IDord-e97544ef8469477ca75b12a99d36b46d
Source noteuspto-grants-1983_08