Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole
Reaktionsgleichung
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[S:15]Cl)#[N:8]>ClC1C=CC=CC=1>[N:1]1([C:7]2[C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15][N:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 130 °C
Versuchsvorschrift
86.2 g (1.00 mol) of piperazine and 7.5 g of chlorobenzene were placed in a 500 ml four-neck flask equipped with a stirrer, a thermometer, a dropping funnel and a condenser and 42.4 g (0.25 mol) of molten 2-cyanobenzenesulfenyl chloride was added dropwise thereto at about 130° C. over one hour while stirring, followed by stirring for four hours to complete the reaction. The excess piperazine was removed with water, followed by acidification with hydrochloric acid and extraction into the aqueous layer. The aqueous layer was basified with an aqueous sodium hydroxide solution to obtain 40.9 g (m.p.: 89°-90° C.) of 3-(1-piperazinyl)-1,2-benzisothiazole as crystals. The yield starting from 2-cyanobenzenesulfenyl chloride was 74.7%.