HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 903593Erstellt: 24. Oktober 2026
Hydrochloric Acid → N-methyl-N-(4-methoxycarbonylbutyryl)-tryptamine
https://huagongshe.com/de/reaction/903593
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Methyltryptamine | HCID 6088 | — |
| Edukt | Dimethyl Glutarate | HCID 14242 | — |
| Produkt | N-methyl-N-(4-methoxycarbonylbutyryl)-tryptamine | HCID 23336480 | 74,8% |
Reaktionsschritte
8.0 g of dimethyl glutarate were added to 8.70 g of N-methyl-tryptamine (i.e., 3-(2-methylaminoethyl)-indole), and the mixture was heated at 150° C. under reduced pressure for 2 hours. After the reaction was completed, the mixture was acidified with dilute hydrochloric acid and then extracted with ethyl acetate. The extract was washed with water, an aqueous saturated sodium bicarbonate solution and an aqueous saturated sodium chloride solution, successively. The washed extract was dried and evaporated under reduced pressure to remove solvent. The residue thus obtained was recrystallized from a mixture of ethyl acetate and n-hexane. 11.3 g of N-methyl-N-(4-methoxycarbonylbutyryl)-tryptamine (i.e., 3-[2-(N-methyl-4-methoxycarbonylbutanamido)ethyl]-indole) were thereby obtained. M.p. 101°-102° C. Yield: 70%
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04228168 |
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| Quelldatensatz | uspto-grants-1980_10 |
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| ORD ID | ord-6716595877b943c0bcbc809cc2a611a5 |
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| Quellennotiz | uspto-grants-1980_10 |
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