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HRID 403608Erstellt: 24. Oktober 2026
3H-Indole, 2,3,3-trimethyl- → 2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chloride
https://huagongshe.com/de/reaction/403608
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3H-Indole, 2,3,3-trimethyl- | HCID 15427 | — |
| Edukt | N-(3-bromopropyl)triethylammonium chloride | HCID 89781116 | — |
| Produkt | 2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chloride | HCID 89781580 | 36% |
Reaktionsschritte
Freshly distilled 2,3,3-trimethylindolenine (0.53 g, 3.3 mmol) and N-(3-bromopropyl)triethylammonium chloride (1.01 g, 3.9 mmol) were mixed in the thick-wall tube and placed under an argon atmosphere. The mixture was then heated at 140° C. for 1.5 h, giving a deep red viscous product, which solidified to a glass on cooling. It was ground to a powder under acetone; product was collected by filtration, triturated 3 times with 10 mL portions of acetone and dried under vacuum to give 0.45 g (36%) of 2,3,3-trimethyl-1-(3-triethylammoniopropyl)-3H-indolium bromide chloride as a white powder. δH (200 MHz, DMSO-d6) 8.10 (1H, d, 6.7 Hz, arom.), 7.87 (1H, d, 5.8 Hz, arom.), 7.75-7.58 (2H, m, arom.), 4.56 (2H, t, 7.3 Hz, N+CH2), 3.27 (6H, q, 6.0 Hz, N+(CH2)3), 2.91 (3H, s, CH3), 2.34-2.10 (2H, m, N+CH2), 1.56 (6H, s, (CH3)2) 1.36-1.05 (11H, m, CH2, (CH3)3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08748446B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-42be14ad864246099ad5c240b809973e |
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| Quellennotiz | uspto-grants-2014_06 |
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