HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Methylimidazo[1,2-a]pyridine-8-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13900241 | HCID 13900241 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Methylimidazo[1,2-a]pyridine-8-methanol | HCID 13900330 | — |
Reaction Steps
To a stirred suspension of 56.8 g (0.36 mol) 2-methyl-8-formylimidazo[1,2-a]pyridine in 400 ml isopropanol at 0°is added in portions 8 g (0.21 mol) sodium borohydride. The reaction mixture is stirred at room temperature for an additional 2 hours. The excess sodium borohydride is decomposed by the addition of distilled waterand the solution concentrated under reduced pressure at 50° C. The residue is dissolved in water and extracted with chloroform. The chloroform extracts are combined and dried over anhydrous sodium sulfate. Following filtration, the chloroform is removed under reduced pressure to give 2-methyl-8-hydroxymethylimidazo[1,2-a]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450164 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-0cd4031f60504719a0755472e7bc360a |
| Source note | uspto-grants-1984_05 |