HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583273Generated: October 27, 2026
Carbon Disulfide → 3-{2-[(2-Hydroxyethyl)sulfanyl]ethyl}-4-methyl-1,3-thiazole-2(3H)-thione
https://huagongshe.com/reaction/1583273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-((2-Aminoethyl)thio)ethanol | HCID 90457 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-{2-[(2-Hydroxyethyl)sulfanyl]ethyl}-4-methyl-1,3-thiazole-2(3H)-thione | HCID 20260303 | — |
Reaction Steps
In 500 ml of ethanol, 24.2 g of (2) and 24.7 ml of triethylamine were dissolved and cooled to 0° C. Thereto, 16.8 g of carbon disulfide was added dropwise. The resulting mixture was allowed to stand for 2 hours at a room temperature and further, for an additional 30 minutes at 50° C. to conduct the reaction. Then, the reaction mixture was cooled to 0° C. again. Thereto, 19.4 g of chloroacetone was added dropwise. The reaction was run by keeping the temperature of the reactionsystem at a room temperature for 1 hour and further, at 40° C. for an additional 2 hours. At the conclusion of the reaction, the solvent was removed by distillation under reduced pressure, and water was added to the residue. The reaction product was extracted with ethyl acetate, washed with water three times, and dried over anhydrous sodium sulfate. Upon the removal of ethyl acetate from the extract by distillation, (1) was obtained as an oily sub stance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04551419 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-33c03bfc644b4b1c85cfe0d37875d43b |
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| Source note | uspto-grants-1985_11 |
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