Reaktionsgleichung
Cl[CH2:2][CH2:3][CH2:4][C:5]1([C:18]#[N:19])[C:17]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[C:11]2[C:6]1=[CH:7][CH:8]=[CH:9][CH:10]=2.[NH:20]1[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1.[I-].[K+]>>[O:23]1[CH2:24][CH2:25][N:20]([CH2:2][CH2:3][CH2:4][C:5]2([C:18]#[N:19])[C:17]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[C:11]3[C:6]2=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH2:21][CH2:22]1Komponenten
Versuchsvorschrift
9-Cyanofluorene was reacted with sodium amide and 1,3-dichloropropane to give 9-(3chloropropyl)-9-cyanofluorene. A solution of 10.0 g. of 9-(3-chloropropyl)-9-cyanofluorene in 200 ml. of morpholine containing 2.0 g. of potassium iodide was stirred at 160° C. for sixteen hours. After cooling the reaction mixture to room temperature, the solution was diluted with 500 ml. of water, and the aqueous mixture was extracted several times with ethylacetate. The organic extracts were combined, washed with water, and the product was extracted therefrom into 0.6 N hydrochloric acid. The aqueous acid layer was separated and made alkaline by the addition of 10 percent sodium hydroxide solution. The alkaline solution was extracted with fresh ethyl acetate, and the extracts were combined, washed with water and dried. Removal of the solvent by evaporation under reduced pressure provided 9-(3-morpholinopropyl)-9-cyanofluorene.
Aufarbeitung
- additionthe solution was diluted with 500 ml
- extractionof water, and the aqueous mixture was extracted several times with ethylacetate
- washwashed with water
- extractionthe product was extracted
- customThe aqueous acid layer was separated
- additionby the addition of 10 percent sodium hydroxide solution
- extractionThe alkaline solution was extracted with fresh ethyl acetate
- washwashed with water
- customdried
- customRemoval of the solvent
- customby evaporation under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-64195521c8d24320bf4661885157e718
- Quelldatensatz
- uspto-grants-1983_05
- Patentnummer
- US04382093
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