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HRID 267538Erstellt: 26. Oktober 2026

Pyridine → Zinc Bis(2,2-dimethyloxazolidine-3-carbodithioate)

https://huagongshe.com/reaction/267538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktCarbon DisulfideHCID 6348—
EduktZinc AcetateHCID 11192—
Edukt2,2-Dimethyl-oxazolidineHCID 550697—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
ProduktZinc Bis(2,2-dimethyloxazolidine-3-carbodithioate)HCID 21453996—

Reaktionsschritte

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 C12H20N2O2S 4 Zn: C, 34.50; H, 4.79; N, 6.71; Zn, 15.67%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03943143
Quelldatensatzuspto-grants-1976_03
ORD IDord-926e339cb26d43fe879fbd7d6cc04b66
Quellennotizuspto-grants-1976_03