HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1,7-dicarbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1-formyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole | HCID 15077730 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1,7-dicarbaldehyde | HCID 17961974 | — |
Reaction Steps
To phosphoric trichloride (136 ml) was added N,N-dimethylformamide (339 ml) under ice-cooling, and the mixture was stirred under ice-cooling for 30 minutes. To the mixture was added a solution of 2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1-carbaldehyde (100 g) in N,N-dimethylformamide (200 ml), and the mixture was stirred at 80° C. for 1.5 hours. The reaction mixture was carefully added to a mixture of ethyl acetate and water under ice-cooling, and the mixture was adjusted to pH 6. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with diisopropyl ether and dried in vacuo to give 2,3-dihydro-1H-imidazo[1,2-b]pyrazole-1,7-dicarbaldehyde (102 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179801B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-d08d4fc5ddd44599a6c2874947a805b5 |
| Source note | uspto-grants-2007_02 |