Reaktion #47833

Reaktionsgleichung

triethylamine

cyclohexylamine

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid

6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic Acid

water

→

titled compound

Ausbeute 20.0%

6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic Acid Cyclohexylamide

Ausbeute 20.0%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeat 10° C
2. 2
   workup.STIRRINGstirred for additional 1 hr in a water bath
3. 3
   Sonstigethe reaction
4. 4
   Waschenthe mixture washed with sodium bicarbonate
5. 5
   Extraktionextracted with dichloromethane
6. 6
   SonstigeThe organic layer was separated
7. 7
   Trocknendried over anhydrous MgSO4
8. 8
   Einengenconcentrated under a reduced pressure
9. 9
   SonstigeThe resulting residue was purified by flash chromatography

Vorschrift

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid (100 mg, 0.38 mmol) obtained in Step 2 was dissolved in dichloromethane, and triethylamine (175 μl, 1.25 mmol) and cyclohexylamine (43 μl, 0.38 mmol) were added thereto at 10° C. Then, bis(2-oxo-3-oxazoline)phosphoryl chloride (100 mg, 0.38 mmol) was further added thereto, stirred for 10˜20 minutes at RT, and then stirred for additional 1 hr in a water bath. After water was added to complete the reaction, the mixture washed with sodium bicarbonate and extracted with dichloromethane. The organic layer was separated, dried over anhydrous MgSO4, concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 26 mg of the titled compound (yield: 20.0%) as a red solid.

Quelle