HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Imidazo[1,2-a]pyridine-6-carbaldehyde | HCID 7164582 | — |
| Catalyst | Butylamine | HCID 8007 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine | HCID 53915568 | 11.9% |
Reaction Steps
In 40 ml of ethanol, 6.9 g of 6-imidazo[1,2-a]pyridinecarbaldehyde was stirred under reflux for 14 hours, together with 10.6 g of nitroethane and 30 drops of n-butyl amine. Then, a small quantity of ethyl amine was added thereto and the mixture was stirred under reflux for further 18 hours. After insoluble matter was removed by filtration upon heating, 50 ml of ethanol and 150 ml of ether were further added to remove insoluble matter by filtration. The solvent was removed by distillation under reduced pressure and the residue was recrystallized twice from ethanol to obtain 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791202 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-b67346cabdc447b4ae4a5cb1e2f69ef5 |
| Source note | uspto-grants-1988_12 |