Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436287Generated: October 26, 2026

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

https://huagongshe.com/reaction/436287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCarbon DisulfideHCID 6348—
ReactantZinc AcetateHCID 11192—
Reactant2,2-Dimethyl-oxazolidineHCID 550697—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductZinc Bis(2,2-dimethyloxazolidine-3-carbodithioate)HCID 21453996—

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04008244
Source datasetuspto-grants-1977_02
ORD IDord-2a01b3882ec84cc6ae7beccbd576ba85
Source noteuspto-grants-1977_02