HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720063Generated: October 31, 2026
Potassium Carbonate → HCID 15342553, compound
https://huagongshe.com/reaction/1720063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Hydroxyindole | HCID 16054 | — |
| Reactant | HCID 15342547 | HCID 15342547 | — |
| Reactant | HCID 22419957 | HCID 22419957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 15342553 | HCID 15342553 | — |
Reaction Steps
Synthesis of 3-(2-aminoethyl)-5-(5-phenylpentyloxy)indole was based on the protocols of example 1. A stirred mixture of 5-hydroxyindole (0.5 g, 3.8 mmol), anhydrous K2CO3, (2-bromopentyl)benzene, and a catalytic amount of KI in 2-butanone (40 ml) was heated at reflux overnight under nitrogen. After allowing to cool to room temperature, the reaction mixture was filtered, the flitrate was then concentrated under reduced pressure to give an oil. The oil was taken up in CH2Cl2 (50 ml) and washed successively with 2N-NaOH (1×20 ml) and water (1×20 ml). The organic portion was dried (MgSO4) and the solvent was removed under reduced pressure to give an oil. The oil was purified by column chromatography using a solvent system of CH2Cl2 /Hexane (40:60) to give 5-(5-phenylpentyloxy)indole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05504101 |
|---|
| Source dataset | uspto-grants-1996_04 |
|---|
| ORD ID | ord-f4376d5926e94592a510a1c4af1cea29 |
|---|
| Source note | uspto-grants-1996_04 |
|---|