HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17622Erstellt: 23. Oktober 2026
Methyl iodide → tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamate
https://huagongshe.com/de/reaction/17622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Tert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamate | HCID 15630117 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamate | HCID 68584969 | 96,1% |
Reaktionsschritte
Tert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamate (2.0 g, 4.24 mmol) was dissolved in N,N-dimethylformamide (40 ml), and at 0° C., methyl iodide (527 μl, 8.47 mmol) and then sodium hydride (55%, w/w), (277 mg, 6.35 mmol) were added. With gradually warming from 0° C. up to room temperature, this was stirred for 24 hours. At 0° C., aqueous saturated ammonium chloride solution was added to the solution, followed by stirring at the same temperature for 30 minutes. The solution was extracted three times with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=99:1, v/v) to obtain a colorless oil (1.982 g, 96%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737166B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-6e43b11caf5d4fa8a96eac542119e500 |
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| Quellennotiz | uspto-grants-2010_06 |
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