HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422010Generated: October 29, 2026
Potassium Carbonate → HCID 178526848, compound
https://huagongshe.com/reaction/1422010
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-nitrothiazole | HCID 18211 | — |
| Reactant | HCID 178518948 | HCID 178518948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178526848 | HCID 178526848 | 18.7% |
Reaction Steps
The title compound was prepared by the general method described by Potts, K.T.(1961) Chem. Rev. 61:87. 4-Phenyl-3-thiosemicarbazide (4.18 g) (Aldrich) was dissolved in 50 mL of pyridine and treated with 2.71 g of ethyl chloroformate at 0° C. The reaction was stirred for 2 hours and then refluxed for 18 hours. Evaporation of the solvent and trituration with water gave 2.5 g of 3-hydroxy-5-mercapto-4-phenyl-1,2,4-triazole. 3-Hydroxy-5-mercapto-4-phenyl-1,2,4-triazole (1.93 g) was stirred in 10 mL of ethanol with 1.1 equivalent of potassium carbonate in 10 mL ethanol for one hour and then reacted with 2.09 g of 2-bromo-5-nitrothiazole as in Example 1. Crystallization from ethanol and water gave 0.6 g of 3-hydroxy-5-[(5-nitrothiazol-2-yl)mercapto]-4-phenyl-1,2,4-triazole, a dark yellow solid, M.P. 188-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080772 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-9194532345414312befee4bd78aa3015 |
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| Source note | uspto-grants-2000_06 |
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