HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507365Erstellt: 24. Oktober 2026
Dimethylformamide → Indole-5-carbonitrile, 3-(2-dimethylaminoethyl)-
https://huagongshe.com/de/reaction/507365
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 5-Bromo-N,N-Dimethyltryptamine | HCID 360252 | — |
| Katalysator | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Katalysator | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Indole-5-carbonitrile, 3-(2-dimethylaminoethyl)- | HCID 28511 | 84% |
Reaktionsschritte
Under an inert atmosphere a flask is charged with [2-(5-bromo-1H-indol-3-yl)-ethyl]-dimethyl-amine (Example 3) (1.0 g, 3.74 mmol), zinc cyanide (0.235 g, 2 mmol), Pd2(dba)3xCHCl3 (0.194 mg, 5 mol %), dppf (bis-diphenylphosphino ferrocene) (0.207 g, 0.374 mmol, 10 mol %), and DMF (12 mL). The orange slurry is heated to 110° C. and stirred for 21 hours. To the black suspension, which has formed, THF (100 mL) is added, and this is extracted with 1 N NaOH (100 mL). The organic layer is washed with water twice (50 mL each), dried and removal of the solvent gives the title product (0.67 g, 84%) as brown solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07786156B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-09bc7caaf0df4d24a634d17d0e98d023 |
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| Quellennotiz | uspto-grants-2010_08 |
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