HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 67273365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 66600637 | HCID 66600637 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67273365 | HCID 67273365 | 76.5% |
Reaction Steps
To a solution of 0.283 g of ethyl 6-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylate in 2 mL of ethanol is added 1 mL of 1 N sodium hydroxide. The reaction mixture is refluxed for 3 hours. After cooling, the reaction medium is acidified with acetic acid. The solid formed is filtered off, washed with water and then dried under vacuum to give 0.195 g of 6-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylic acid in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902219B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-73ca14a05fd142edbf21c4cf939b0e66 |
| Source note | uspto-grants-2011_03 |