Reaktion #46175

Reaktionsgleichung

bis(2-oxo-3-oxazolidinyl)phosphinic chloride

Triethylamine

cyclohexylamine

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate

hydrochloric acid

→

title compound

Ausbeute 59.8%

3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate cyclohexylamide

Ausbeute 59.8%

Lösungsmittel

water

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeat 10° C
2. 2
   workup.WAITfollowed by additional 1 hour at 10° C
3. 3
   Sonstigethe reaction, pH
4. 4
   WaschenThe mixture was washed with brine
5. 5
   Extraktionextracted with dichloromethane
6. 6
   TrocknenThe extract was dried over anhydrous sulfonate sulfate
7. 7
   Einengenconcentrated
8. 8
   Sonstigethe resulting residue was purified by column chromatography (ethyl acetate:hexane=1:9˜2:8)

Vorschrift

3-Phenyl-6-(3-phenylpropyloxy)-1-oxo-1H-indene-2-carboxylate (200 mg, 0.52 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (240 μl, 1.72 mmol) and cyclohexylamine (59 μl, 0.52 mmol) were added thereto at 10° C. Then, after adding bis(2-oxo-3-oxazolidinyl)phosphinic chloride (137 mg, 0.52 mmol), the reaction mixture was stirred for about 20 min at room temperature followed by additional 1 hour at 10° C. After the water was added thereto to complete the reaction, pH was adjusted to 1˜1.5 with 4N hydrochloric acid. The mixture was washed with brine, and extracted with dichloromethane. The extract was dried over anhydrous sulfonate sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:9˜2:8) to obtain the title compound (yield 59.8%) as a red solid.

Quelle