HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfate → (1-Methyl-1H-indol-6-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Methyl N-methylindole-6-carboxylate | HCID 639843 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1-Methyl-1H-indol-6-yl)methanol | HCID 18673032 | 79.3% |
Reaction Steps
A solution of 1-methyl-1H-indole-6-carboxylic acid methyl ester (Example 15; 2.52 g, 13.3 mmol) in diethyl ether (50 mL) was added to a suspension of lithium aluminum hydride (0.50 g, 13.2 mmol) in diethyl ether (50 mL) and the mixture was stirred at room temperature for 5 h. Saturated Na2SO4 solution was added (˜5 mL) and the mixture was stirred at room temperature for 30 min, then filtered and the filtrate was dried (MgSO4), overnight. The mixture was filtered and evaporated to furnish 1-methyl-1H-indole-6-methanol (1.70 g, 79% yield) as a colorless oil that solidified on standing, mp 47-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515124B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-98549dc4656e44e58b273e790cfdedd8 |
| Source note | uspto-grants-2003_02 |