HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1163909Erstellt: 24. Oktober 2026
N-Ethyltryptamine → N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine
https://huagongshe.com/de/reaction/1163909
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Ethyltryptamine | HCID 6092 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Benzyloxycarbonylglycine | HCID 14349 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine | HCID 20513176 | 101,6% |
Reaktionsschritte
30 ml of anhydrous tetrahydrofuran and 1.05 g of triethylamine are added to 2.17 g of N-benzyloxycarbonyl-glycine, and 1.43 g of isobutyl chloroformate are added dropwise thereto at -15° C. under stirring. A solution of 1.96 g of N-ethyl-tryptamin (i.e., 3-(2-ethylamino)ethylindole) in 40 ml of anhydrous tetrahydrofuran is added dropwise to the mixture at the same temperature, and said mixture is stirred at 0° C. for one hour and further stirred at room temperature for 16 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (oil) is purified by silica gel chromatography (Solvent: ethyl acetate-chloroform (1:1). 4.0 g of N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine are thereby obtained as a colorless oil. Yield: 100%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04367230 |
|---|
| Quelldatensatz | uspto-grants-1983_01 |
|---|
| ORD ID | ord-c07ad14976464c3099faf93d61d2dd8f |
|---|
| Quellennotiz | uspto-grants-1983_01 |
|---|