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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chloro-2(1H)-pyrimidinone | HCID 108578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2(3H)-Furanone, dihydro-4-methylene- | HCID 12303360 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20491782 | HCID 20491782 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04399140 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-e97544ef8469477ca75b12a99d36b46d |
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| Source note | uspto-grants-1983_08 |
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