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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl iodideHCID 11166—
Edukttert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614133—
KatalysatorHCID 178418778HCID 178418778—
LösungsmittelTolueneHCID 1140—
Produkttert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614132—

Reaktionsbedingungen

Temperatur65 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745484B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-71e22a70ba924d01bbdb8094577fa4cf
Quellennotizuspto-grants-2010_06