HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(2-Phenylethyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22419955 | HCID 22419955 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2-Phenylethyl)-1H-indole | HCID 13245155 | — |
Reaction Steps
To a solution of the 3-ethyloxycarbonyl-5-phenethylindole (0.4 g, 1.5 mmol) in EtOH 95% (10 ml) was added an excess of KOH (0.5 g) and the reaction mixture was heated at reflux for 2 h. The solution was acidified with 1N HCl (10 ml) and the precipitated material was collected by filtration. The solid was washed well with H2O (2×10 ml) to give the corresponding acid. The acid (0.3 g, 1.2 mmol) was immersed in an oil bath and then heated at about 235°-240° C. for 15 min to give a brown syrup. Distillation of the oil under high vacuum provided 5-phenethylindole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05504101 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-e2f155c7302741edac24e313280b1488 |
| Source note | uspto-grants-1996_04 |