HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20042Erstellt: 23. Oktober 2026
Allyl iodide → tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamate
https://huagongshe.com/de/reaction/20042
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl iodide | HCID 11166 | — |
| Edukt | tert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamate | HCID 86614133 | — |
| Katalysator | HCID 178418778 | HCID 178418778 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamate | HCID 86614132 | — |
Reaktionsschritte
To a solution of tert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamate (0.125 g, 0.6 mmol; see: Kurokawa, N.; Ohfune, Y. Tetrahedron 1993, 49, 6195) in toluene (6 mL), was added allyliodide 0.3 mL, 3 mmol) followed by silver(I) oxide (0.7 g, 3 mmol). The solution was stirred at 65° C. in a darkened hood for a period of 15 h. The mixture was then cooled to ambient temperature, filtered through Celite, washed with CH2Cl2, and conc. in vacuo. Purification on SiO2 (10-20% EtoAc/Hexanes) gave the title compound as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745484B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-71e22a70ba924d01bbdb8094577fa4cf |
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| Quellennotiz | uspto-grants-2010_06 |
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