HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methoxytryptamine → N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)-3-propoxybenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methoxytryptamine | HCID 1833 | — |
| Reactant | 3-Propoxybenzaldehyde | HCID 2760469 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)-3-propoxybenzylamine | HCID 21071638 | — |
Reaction Steps
Combine 3-propoxybenzaldehyde (14.05 g, 0.0856 mole) and 5-methoxytryptamine (13.64 g, 0.0717 mole) in 390 mL absolute EtOH. Add molecular sieves (19.2 g) and heat the suspension to reflux. After 4 hours, cool to room temperature and add NaBH4 (37.32 g, 0.2146 mole) in 3 portions. Stir the mixture for 1 hour at room temperature, filter, evaporate the filtrate to a mass of about 100 g, add water and dichloromethane. After separation, wash the aqueous phase with dichloromethane, combine the organic layers, dry over MgSO4, filter, evaporate the solvent in vacuo to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157488B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-50de1524f45444ebb45edf9ac5088a5b |
| Source note | uspto-grants-2007_01 |