HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (2-tert-butyl-5-nitro-1H-indol-7-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 2-tert-butyl-5-nitro-1H-indole-7-carboxylate | HCID 53436897 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-tert-butyl-5-nitro-1H-indol-7-yl)methanol | HCID 59129235 | 73% |
Reaction Steps
To a solution of methyl 2-tert-butyl-5-nitro-1H-indole-7-carboxylate (6.15 g, 22.3 mmol) and dichloromethane (30 ml) was added DIBAL-H (1.0 M, 20 mL, 20 mmol) at 78° C. The mixture was stirred for 1 h before water (10 mL) was added slowly. The resulting mixture was extracted with EtOAc (120 mL×3). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum to give (2-tert-butyl-5-nitro-1H-indol-7-yl)methanol (4.0 g, 73%), which was used in the next step directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598181B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-2678f9b7c96442448fddf16d9a86ac89 |
| Source note | uspto-grants-2013_12 |