HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267539Generated: October 29, 2026
Carbon Disulfide → HCID 21453991, compound
https://huagongshe.com/reaction/267539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Zinc Acetate | HCID 11192 | — |
| Reactant | HCID 12444283 | HCID 12444283 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21453991 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943143 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-09ef974eeb33450882faf89316753d9b |
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| Source note | uspto-grants-1976_03 |
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