Reaktionsgleichung
[CH3:1][C:2]1([CH3:7])[NH:6][CH2:5][CH2:4][O:3]1.[C:8](=[S:10])=[S:9].N1C=CC=CC=1.C([O-])(=O)C.[Zn+2:21].C([O-])(=O)C>C(Cl)(Cl)Cl.C(O)C>[CH3:1][C:2]1([CH3:7])[N:6]([C:8]([S-:10])=[S:9])[CH2:5][CH2:4][O:3]1.[CH3:1][C:2]1([CH3:7])[N:6]([C:8]([S-:10])=[S:9])[CH2:5][CH2:4][O:3]1.[Zn+2:21]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
While cooling and stirring, 20 g. (0.20 mole) of 2,2-dimethyloxazolidine (preparation described by E. Bergmann et. al., J. Am. Chem. Soc. 75, 358 (1953)) was added to a solution of 15.2 g. (0.20 mole) carbon disulfide in 150 g. pyridine. To the stirring solution was added 18.3 g. (0.10 mole) of anhydrous zinc acetate at 25°-30° C. After standing overnight at room temperature, filtration gave 15.2 g. of the crude product; vacuum-concentration of the filtrate and ethanol-dilution of the residue gave an additional 10.4 g. After combining and vacuum-drying of the crude product at 100° C there was obtained 17.8 g. of the desired carbodithioate melting at 188°- 190° C (decomp.). A small sample, dissolved in hot chloroform and precipitated by hexane (m. 192°-3° C decomp.) had the following analysis: Found: C, 34.22; H, 4.47; N, 6.84; Zn, 15.20%. Calcd for C12H20N2O2S4Zn: C, 34.50; H, 4.79; N, 6.71; Zn, 15.67%.
Aufarbeitung
- temperatureWhile cooling
- additionTo the stirring solution was added 18.3 g
- customat 25°-30° C
- filtrationfiltration
- customgave 15.2 g
- dry with materialvacuum-drying of the crude product at 100° C
- customthere was obtained 17.8 g
- customprecipitated by hexane (m. 192°-3° C decomp.)
Quellen und Nachweise
- ORD-Eintrag
- ord-2a01b3882ec84cc6ae7beccbd576ba85
- Quelldatensatz
- uspto-grants-1977_02
- Patentnummer
- US04008244
Verknüpfte Notizen
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