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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1815942Erstellt: 23. Oktober 2026

Propylene Oxide → (6-Benzyloxy-indol-1-yl)-propan-2-ol

https://huagongshe.com/de/reaction/1815942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropylene OxideHCID 6378—
EduktSodium hydrideHCID 24758—
Edukt6-(benzyloxy)-1H-indoleHCID 260804—
EduktMonobasic potassium phosphateHCID 516951—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(6-Benzyloxy-indol-1-yl)-propan-2-olHCID 22247173—

Reaktionsschritte

To a stirred, cooled (10° C.) suspension of sodium hydride (80.7 g of a 60% dispersion in mineral oil, 2.02 mol) in anhydrous THF (1.9 L) was added a solution of 6-benzyloxyindole (375 g, 1.68 mol) in anhydrous THF (1.9 L) keeping the temperature below 25° C. After 2 h at 10° C., propylene oxide (140 mL, 2.0 mol) was added dropwise keeping the temperature below 25° C. After 48 h at 10° C., propylene oxide (71 mL, 1.0 mol) was added. After 96 h at 10° C., saturated aqueous potassium dihydrogenphosphate (3.8 L) and ethyl acetate (3.8 L) were carefully added, the layers were separated and the aqueous solution was extracted with 3.8 L of ethyl acetate. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to yield a solid (520 g, 110%, contains mineral oil).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06881749B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-432474aceda8463f84b8e7c88480f53e
Quellennotizuspto-grants-2005_04