HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl indole-2-carboxylate → (1H-indol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl indole-2-carboxylate | HCID 73125 | — |
| Reactant | Indole-2-carboxaldehyde | HCID 96389 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1H-indol-2-yl)methanol | HCID 98783 | — |
Reaction Steps
1H-indole-2-carbaldehyde derivatives (1) may be prepared by reduction of commercially available or well known ethyl 1H-indole-2-carboxylate derivatives (12) with a reducing agent such as LAH in an aprotic solvent such as THF to give the corresponding (1H-indol-2-yl)methanol derivative (13). Oxidation with an oxidizing agent such as active manganese dioxide in an aprotic solvent such as DCM gives the desired 1H-indole-2-carbaldehyde derivatives (1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096595B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-151c42a5dc8442b592135c83a737b998 |
| Source note | uspto-grants-2015_08 |