HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657511Generated: October 30, 2026
Hydrogen Bromide → 5-Bromo-3-cyclopropyl-1H-1,2,4-triazole
https://huagongshe.com/reaction/657511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-cyclopropyl-1H-1,2,4-triazol-3-amine | HCID 2758017 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-3-cyclopropyl-1H-1,2,4-triazole | HCID 45791233 | — |
Reaction Steps
5.0 g of 3-amino-5-cyclopropyl-1H-[1,2,4]triazole were dissolved in 30 ml of acetic acid and 20 ml of a 48% aqueous hydrogen bromide solution were added dropwise. Subsequently, a solution of 3.1 g of sodium nitrite in 10 ml of water was added dropwise at 0° C. in the course of 10 min and the mixture was subsequently stirred at 0° C. for 10 min. The suspension thus obtained was added in portions at 0° C. to a suspension of 11.6 g of copper(I) bromide in 20 ml of a 24% aqueous hydrogen bromide solution. Subsequently, it was stirred at room temperature for 1 h, then the mixture was added to 400 ml of a saturated aqueous sodium carbonate solution and precipitated copper compound was filtered off. The mixture was washed with 100 ml of EA, then the phases were allowed to separate and the aqueous phase was extracted a further two times with 100 ml each of EA. The combined organic phases were dried over magnesium sulfate and the solvent was removed in vacuo. 2.5 g of the title compound were obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076324B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-c18b78a92b674d9c9d5f78e93e2a56f4 |
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| Source note | uspto-grants-2011_12 |
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