HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073779Generated: October 26, 2026
Thiophenol → 2-Amino-5-phenylthio-1,3,4-thiadiazole
https://huagongshe.com/reaction/1073779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Amino-5-bromo-1,3,4-thiadiazole | HCID 3650883 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-phenylthio-1,3,4-thiadiazole | HCID 14695068 | 79.4% |
Reaction Steps
In a mixture of 20 ml of water and 30 ml of ethanol, 7.3 g of thiophenol and 4.5 g of potassium hydroxide were added. To this solution, 11.7 g of 2-amino-5-bromo-1,3,4-thiadiazole was added, and the mixture was heated to 82° C. and stirred for 2 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water and n-hexane respectively, dried under reduced pressure, and thus 10.8 g of 2-amino-5-phenylthio-1,3,4-thiadiazole was obtained. m.p. 202°~203° C. Yield 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04971971 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-34899434824746c1807ad518bddb1c91 |
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| Source note | uspto-grants-1990_11 |
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