HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-(4-Carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(4-Ethoxycarbonylbuta-1,3-dienyl)imidazo[1,5-a]pyridine | HCID 53913501 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(4-Carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine | HCID 53838161 | — |
Reaction Steps
To a solution of 200 mg of 5-(4-ethoxycarbonylbuta-1,3-dienyl)imidazo[1,5-a]pyridine in 20 ml of methanol is added 4 ml of 1N sodium hydroxide. The reaction mixture is stirred at room temperature for 18 hours. The methanol is evaporated under reduced pressure and the residue diluted with 20 ml of water and the solution is adjusted to pH 5 with hydrochloric acid. The precipitate is collected to give 5-(4-carboxybuta-1,3-dienyl)-imidazo[1,5-a]pyridine, melting at 243°-245°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588732 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-7e00622a39854c5db365d0fb36351fff |
| Source note | uspto-grants-1986_05 |