HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58337Erstellt: 25. Oktober 2026
1,1'-Carbonyldiimidazole → N3-(tert-butoxycarbonyl)-N3-methyl-N-[4-(triphenylphosphonio) butyl]-beta-alaninamide bromide
https://huagongshe.com/reaction/58337
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | 3-(Methylamino)propanoic acid, N-BOC protected | HCID 2760952 | — |
| Edukt | (4-Aminobutyl)(triphenyl)phosphonium bromide | HCID 10201848 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N3-(tert-butoxycarbonyl)-N3-methyl-N-[4-(triphenylphosphonio) butyl]-beta-alaninamide bromide | HCID 131737008 | 116,1% |
Reaktionsschritte
N-(tert-butoxycarbonyl)-N-methyl-β-alanine (Matrix Scientific, 368 mg, 1.81 mmol) was dissolved in N,N-dimethylformamide (3.7 mL) and treated with N,N-carbonyldiimidazole (308 mg, 1.90 mmol). The reaction mixture was stirred at room temperature for 30 minutes. (4-Aminobutyl)(triphenyl)phosphonium bromide (1.12 g, 2.72 mmol) was added, and the reaction was stirred overnight at room temperature. The reaction was then diluted with methylene chloride and washed with 5% aqueous lithium chloride (3 times), 1N aqueous hydrogen chloride, and saturated sodium bicarbonate. The organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (1.26 g, 100%, 86% pure) as a white foam. Sample was used crude in next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434753B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-cdb50267135e41e7bd059917746c5047 |
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| Quellennotiz | uspto-grants-2016_09 |
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