HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487984Generated: October 30, 2026
Benzyl Bromide → 4-Benzyl-3,5-dibromo-4H-1,2,4-triazole
https://huagongshe.com/reaction/1487984
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178419480 | HCID 178419480 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Benzyl-3,5-dibromo-4H-1,2,4-triazole | HCID 90029181 | 89% |
Reaction Steps
To a solution of 3,5-dibromo-4H-1,2,4-triazole (3.0 g, 13.3 mmol) in DMF (10 mL) at 0° C. was added NaH (60% in mineral oil, 0.58 g, 14.5 mmol) (CAUTION: NaH and DMF can become a runaway reaction. All necessary safety precautions were performed). After the mixture was stirred at 0° C. for 30 minutes, benzyl bromide (1.57 mL, 13.2 mmol) was added. The mixture was stirred at 0° C. for 2 hours, then the mixture was partitioned between EtOAc (150 mL) and water (30 mL). The organic layer was washed with brine (2×30 mL), dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexanes:EtOAc 50:1 to 10:1) to yield 3.71 g (89%) of the title compound as a white solid. m/z (ES+) 316, 318, 320 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-b567d3bf526f44c4afdce7890ac4fe80 |
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| Source note | uspto-grants-2016_08 |
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