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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17886Generated: October 25, 2026

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

https://huagongshe.com/reaction/17886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 178458041HCID 178458041—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
Product6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amideHCID 8661402999%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741323B2
Source datasetuspto-grants-2010_06
ORD IDord-5da6139b69b8451d84463995d522f076
Source noteuspto-grants-2010_06