HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538994Generated: October 26, 2026
Hydrazine → 3-(4-bromo-2-fluorophenyl)-4H-1,2,4-triazole
https://huagongshe.com/reaction/538994
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 178484324 | HCID 178484324 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(4-bromo-2-fluorophenyl)-4H-1,2,4-triazole | HCID 58298331 | 114% |
Reaction Steps
Hydrazine (0.14 mL, 4.4 mmol) was added to a solution of (E)-4-bromo-N-((dimethylamino)methylene)-2-fluorobenzamide (1.105 g, 4.046 mmol) in acetic acid (11 mL). The resulting white suspension was heated to 95-100° C. The resulting solution was stirred at 95-100° C. for 2 hours. The reaction mixture was cooled to ambient temperature and the acetic acid was azeotropically removed in vacuo with multiple additions of heptane. Heptane (10 mL) was added to the residue. The resulting suspension was cooled to 0-5° C. and stirred for 1 hour. The solids were collected by vacuum filtration, rinsed with excess heptane, and dried to afford 5-(4-bromo-2-fluorophenyl)-1H-1,2,4-triazole (1.116 g, 114%) as an off-white solid which was carried on without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865726B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-db5d27b0f18b4f64bf1215309455f401 |
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| Source note | uspto-grants-2014_10 |
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