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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267539Generated: October 29, 2026

Carbon Disulfide → HCID 21453991, compound

https://huagongshe.com/reaction/267539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantZinc AcetateHCID 11192—
ReactantHCID 12444283HCID 12444283—
SolventPyridineHCID 1049—
ProductHCID 21453991HCID 21453991—

Reaction Steps

While cooling and stirring 250 g. of pyridine, 175 g. (1.40 moles) of thiazolidine hydrochloride [preparation described by S. Ratner and H. Clarke, J. Am. Chem. Soc. 59, 200 (1937)] was added. After it had dissolved, 106.4 g. (1.40 mole) of carbon disulfide was added dropwise, followed by 128.5 g. (0.70 mole) of anhydrous zinc acetate. The resulting reaction mixture was stirred at 40° - 50°C for 2 hours. The precipitate was filtered at 5° - 10°C. The crude solid was water-washed and finally freed of pyridine by vacuum-drying at 120°C to give 147.8 g. of the desired product. It gradually decomposed starting at ca. 200°C without a definite final decomposition point. A small sample washed with hot benzene had the following analysis: Found: C, 24.46; H, 2.95; N, 7.31; Zn, 16.58%. Calcd for C8H12N2S6Zn: C, 24.40; H, 3.05; N, 7.12; Zn, 16.62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943143
Source datasetuspto-grants-1976_03
ORD IDord-09ef974eeb33450882faf89316753d9b
Source noteuspto-grants-1976_03