HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl indole-7-carboxylate → (1H-indol-7-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl indole-7-carboxylate | HCID 676694 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1H-indol-7-yl)methanol | HCID 2773460 | — |
Reaction Steps
Solid lithium aluminum hydride (1.0 g) is added in portions over 1 hour to a stirred solution of methyl 7-indolecarboxylate (6.7 g) in tetrahydrofuran (100 ml). The mixture was stirred for a further 2 hours then excess lithium aluminum hydride was destroyed by addition of acetic acid, the mixture is diluted with aqueous sodium hydroxide and extracted with ethyl acetate. The extract is dried and evaporated and the residue is chromatographed on silica in ethyl acetate-hexane (1:9 to 1:2) to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622969 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-2da6b86adf064be687ad7b5c0bee226d |
| Source note | uspto-grants-1997_04 |