HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Aminoethyl)-5-methoxyindole → 6-Hydroxytryptamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Aminoethyl)-5-methoxyindole | HCID 17654 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Hydroxytryptamine | HCID 160463 | 68.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Diisobutylaluminum hydride (1 M in toluene, 15 mL) was slowly added to a suspension of 2-(6-methoxy-1H-indol-3-yl)ethylamine (250 mg) in 20 mL of toluene. The resulting clear solution was refluxed for 10 h, then cooled to 0° C. and quenched by the careful addition of 20 mL of 1:1 methyl alcohol:water. The mixture was stirred for 15 min at rt and filtered to remove the precipitated aluminum salts. The solvent was evaporated to yield 158 mg of 3-(2-amino-ethyl)-1H-indol-6-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084154B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-e5c557f7a27d4624a1960146dfa584ae |
| Source note | uspto-grants-2006_08 |