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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82882Erstellt: 24. Oktober 2026

Cesium carbonate → Ethyl 6-(2-aminoethoxy)-1-benzyl-2,3-dihydro-1H-inden-2-ylcarbamate

https://huagongshe.com/de/reaction/82882

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
Eduktethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamateHCID 66740125—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 6-(2-aminoethoxy)-1-benzyl-2,3-dihydro-1H-inden-2-ylcarbamateHCID 66740622—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A suspension of ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate (620 mg, 1.991 mmol) and caesium carbonate (1298 mg, 3.98 mmol) in acetonitrile (15 ml) was stirred at 80° C. under argon for 1 h, cooled down to 50° C. and tert-butyl 2-bromoethylcarbamate (669 mg, 2.99 mmol)dissolved in acetonitrile was slowly added. Stirred at 80° C. for 2 h. Evaporated acetonitrile, re-dissolved in dichloromethane, washed with water, co-extracted aqueous layer twice with dichloromethane and the combined organic layers were dried, filtered and evaporated and purified by flash silica gel chromatography on 40 g SiO2-cartridge using 30% ethyl acetate in cyclohexane to afford the titled compound as a brown oil. m=624 mg

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846743B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-af87164024a443faa033e989b00669ec
Quellennotizuspto-grants-2014_09