Reaktionsgleichung
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][OH:13].[N+]([C:18]1[CH:19]=[C:20]([C:26]#[N:27])[C:21](=[CH:24][CH:25]=1)[C:22]#[N:23])([O-])=O.[C:28](=[O:31])([O-])[O-].[K+].[K+].Cl>CS(C)=O>[C:26]([C:20]1[CH:19]=[C:18]([CH:25]=[CH:24][C:21]=1[C:22]#[N:23])[O:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][O:31][C:28]1[CH:25]=[CH:24][C:21]([C:22]#[N:23])=[C:20]([C:26]#[N:27])[CH:19]=1)#[N:27]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 1,12-dodecanediol (20.4 g, 0.10 mol), 4-nitrophthalonitrile (35 g, 0.20 mol), anhydrous potassium carbonate (69 g, 0.50 mol) and 180 ml of dimethyl sulfoxide was heated at 70°-75° C. for 6 hours under a nitrogen atmosphere. The potassium carbonate was added in three portions. After cooling, the content was slowly poured into 500 ml of cold dilute (2 N) hydrochloric acid. The aqueous solution was extracted with four, 100 ml portions of chloroform. The combined extract was washed several times with water, charcoaled, dried over anhydrous sodium sulfate and concentrated to afford 42 g of crude product. Recrystallization from ethanol-water yielded 24.4 g (54%), m.p. 104°-107° C. of 1,12-bis(3,4-dicyanophenoxy) dodecane.
Aufarbeitung
- temperaturewas heated at 70°-75° C. for 6 hours under a nitrogen atmosphere
- temperatureAfter cooling
- additionthe content was slowly poured into 500 ml
- extractionThe aqueous solution was extracted with four, 100 ml portions of chloroform
- extractionThe combined extract
- washwas washed several times with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated
- customto afford 42 g of crude product
- customRecrystallization from ethanol-water
Quellen und Nachweise
- ORD-Eintrag
- ord-a96b19dd6bc84d4b885cea11d2a42883
- Quelldatensatz
- uspto-grants-1980_10
- Patentnummer
- US04226801
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