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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17886Erstellt: 25. Oktober 2026

Triphenylphosphine → 6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide

https://huagongshe.com/reaction/17886

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-MorpholinoethanolHCID 61163—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
EduktHCID 178458041HCID 178458041—
LösungsmittelBenzeneHCID 241—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amideHCID 8661402999%

Reaktionsschritte

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide (7.0 g, 22.78 mmol) was dissolved in tetrahydrofuran:benzene (150 ml:50 ml). Then, hydroxyethylmorpholine (3.59 g, 27.33 mmol) and triphenyl phosphine (7.17 g, 27.33 mmol) were added thereto. When the temperature was adjusted to 0° C., diisopropyl azodicarboxylate (5.53 g, 27.33 mmol) was added dropwise to the mixture followed by stirring for 2 hours at room temperature. The mixture was washed with brine and extracted with ethyl acetate. The separated organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide (9.5 g, yield 99%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741323B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5da6139b69b8451d84463995d522f076
Quellennotizuspto-grants-2010_06