HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → Ethyl 2,3-dihydropyrazolo[5,1-b]oxazole-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178469373 | HCID 178469373 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2,3-dihydropyrazolo[5,1-b]oxazole-6-carboxylate | HCID 69588863 | 43.7% |
Reaction Steps
To the stirred suspension of ethyl 5-hydroxy-1H-pyrazole-3-carboxylate (10.34 g, 0.66 mol) and 36.62 g of potassium carbonate in 500 ml of acetonitrile was added 13.68 g of 1,2-dibromoethane, and refluxed for 16 hours. The reaction mixture was allowed to cool to room temperature, then filtered, the solid was washed with acetonitrile. The filtrate was concentrated to an oil. The residue was dissolved in ethyl acetate and extracted with water. The organic phase was dried over MgSO4 and evaporated to dryness. 5.80 g of the desired product was obtained (48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112582B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-41f40700d771491b841b390806a90b77 |
| Source note | uspto-grants-2006_09 |