HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 8-Acetoxy-2-methylimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methylimidazo[1,2-a]pyridin-8-ol | HCID 820953 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Acetoxy-2-methylimidazo[1,2-a]pyridine | HCID 18321926 | 102% |
Reaction Steps
A mixture of 8-hydroxy-2-methylimidazo[1,2-a]pyridine (10 g), acetic anhydride (10.3 g) and pyridine (10.7 g) in anhydrous dichloromethane (100 ml) was stirred for 1 hour at ambient temperature and allowed to stand overnight. The 30 mixture was washed with water, and the organic layer was separated. The aqueous layer was neutralized with sodium bicarbonate and extracted with chloroform. The combined organic layers were washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated in vacuo to give 8-acetoxy-2-methylimidazo[1,2-a]pyridine (13.1 g) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008229 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-c73c14e2cff948938980e69f1e0397eb |
| Source note | uspto-grants-1999_12 |