HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436289Generated: October 31, 2026
Carbon Disulfide → HCID 21454007, compound
https://huagongshe.com/reaction/436289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Zinc Acetate | HCID 11192 | — |
| Reactant | 2,2-Dimethyl-1,3-thiazolidine--hydrogen chloride (1/1) | HCID 120386 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21454007 | HCID 21454007 | — |
Reaction Steps
While cooling and stirring at 10° C, 76.8 g. (0.50 mole) 2,2-dimethylthiazolidine hydrochloride [preparation described by B. Sweetman et al. J. Med. Chem. 12, 888 (1969)] was added to a mixture of 30 ml isopropanol and 101 g. (1.00 mole) triethylamine. Likewise, 38.0 g. (0.50 mole) of carbon disulfide was gradually added, followed by 45.8 g. (0.25 mole) of anhydrous zinc acetate. After standing ovenight at room temperature, the precipitate was filtered, twice water-washed with 1 liter portions of water and air-dried to give 80.5 g. of the yellow product melting at 148° - 153° C (decomp.) and having the following analysis: Found: C, 31.51; H, 4.70%. Calcd for C12H20N2S6Zn: C, 32.04; H, 4.45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04008244 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-46cd78d527ee4463aa74dbb2369a644b |
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| Source note | uspto-grants-1977_02 |
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