HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminum hydride → 5-(Hydroxymethyl)-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Ethyl 1H-benzimidazole-6-carboxylate | HCID 13505555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Hydroxymethyl)-1H-benzimidazole | HCID 13505556 | — |
Reaction Steps
To a cooled (0° C.) suspension of ethyl-benzimidazole-5-carboxylate (4.76 g, 25 mmol) in CH2Cl2 (100 mL) was added a 1 M solution of DIBAL in CH2Cl2 (100 mL) and the mixture was stirred for 4 h. The reaction was quenched by the sequential addition of MeOH (8 mL), 1 M NaOH (16 mL), and 30% sodium potassium tartrate (40 mL). The mixture was warmed to RT and filtered, and the solid residue was washed with CH2Cl2. The filtrate was concentrated in vacuo to afford the title compound as a brown solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610692B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-2ed67267f49b4afa92a5a77e5d9340aa |
| Source note | uspto-grants-2003_08 |