HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 7-Ethylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 4-Ethylpyridin-2-amine | HCID 118425 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Ethylimidazo[1,2-a]pyridine | HCID 18184463 | 98.6% |
Reaction Steps
A mixture of 4-ethylpyridin-2-amine (3.21 g, 8.19 mmol), and chloroacetaldehyde (50% aqueous solution, 2.6 ml, 10.5 mmol) in EtOH (10 ml) was refluxed vigorously for 12 hours. The reaction mixture was concentrated, and the residue was suspended in saturated aqueous sodium bicarbonate solution. The aqueous mixture was extracted with CH2Cl2 and EtOAc, and the combined organic extracts were dried over Na2SO4, filtered and concentrated to afford the desired product (1.18 g, 98% yield) as a viscous oil. MS APCI (+) m/z 147.2 (M+1) detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138181B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-a14ef65495744592aceb2fbe75dcfb13 |
| Source note | uspto-grants-2012_03 |