HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127349Generated: October 31, 2026
Phenacyl bromide → 2-phenylimidazo[1,2-a]pyrimidine
https://huagongshe.com/reaction/127349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 2-Aminopyrimidine | HCID 7978 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-phenylimidazo[1,2-a]pyrimidine | HCID 204149 | 102.4% |
Reaction Steps
A mixture of 9.5 g of 2-aminopyrimidine (0.1 mole), 20 g of ω-bromoacetophenone (0.1 mole) and 200 ml of 95% ethanol is refluxed for three hours and then heated at 60° for an additional 12 hours with stirring. After cooling, the reaction product is condensed to a thick liquid by evaporating it in a rotary evaporator. The residue is mixed with 500 ml of methylene chloride and 100 ml of 3 N sodiumhydroxide solution. The mixture is stirred for 10 minutes and then separated in two layers in a separatory funnel. The lower layer (solvent) is collected, washed with 100 ml of water and then evaporated to dryness under reduced pressure. The residue is washed with 2-propanol on a glass filter and dried in vacuum to yield about 20 g of 2-phenylimidazo(1,2-a)pyrimidine, m.p. 200° to 202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255573 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-ede9d9776f1343119a97d52b842b7bd8 |
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| Source note | uspto-grants-1981_03 |
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