HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Hydroxymethylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl indole-6-carboxylate | HCID 639844 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium | HCID 5360545 | — |
| Product | 6-Hydroxymethylindole | HCID 2773459 | — |
Reaction Steps
Lithium aluminium hydride (3.48 g, 91.70 mmol) was suspended in sodium-dried tetrahydrofuran (150 ml). The suspension was stirred under a nitrogen atmosphere. Methyl-(indol-6-yl)methanoate (8.0 g, 45.7 mmol) was dissolved in dry tetrahydrofuran (50 ml) and added dropwise to the lithium aluminium hydride suspension. The mixture was stirred at ambient temperature for three hours. Water (10 ml) was added dropwise, followed by 2N hydrogen chloride (30 ml). The mixture was extracted with diethyl ether (3×150 ml) to yield a light purple oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563147 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-59a092bf5ca742a0a637c686b8d64f1d |
| Source note | uspto-grants-1996_10 |