HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478251Generated: October 30, 2026
Water → 1-(3'-bromobiphenyl-2-yl)-1H-[1,2,4]triazole
https://huagongshe.com/reaction/478251
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 1-(2-tributylstannylphenyl)-1H-[1,2,4]triazole | HCID 18001302 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3'-bromobiphenyl-2-yl)-1H-[1,2,4]triazole | HCID 18001279 | — |
Reaction Steps
To a degassed solution of 1-(2-tributylstannylphenyl)-1H-[1,2,4]triazole (300 mg, 0.7 mmol) in N,N-dimethylformamide (5 ml) was added 1,3-dibromobenzene (0.17 ml, 1.4 mmol), tetrakis(triphenylphosphine)palladium(0) (40 mg, 35 μmol), lithium chloride (293 mg, 6.9 mmol), then copper(I) iodide (13 mg, 69 μmol), and the mixture was heated at 80° C. for 5 h. The reaction was cooled to ambient temperature then poured into water (20 ml) and extracted with dichloromethane (3×20 ml). The combined organic phases were dried over anhydrous magnesium sulfate, filtered and evaporated to dryness. Purification by chromatography on silica gel eluting with dichloromethane on a gradient of methanol (0-1%), then by preparative thin-layer chromatography on silica gel using 5% methanol in dichloromethane as eluent, gave 1-(3′-bromobiphenyl-2-yl)-1H-[1,2,4]triazole as a colourless gel: m/z (ES+) 300, 302 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642229B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-682383c6bf5042b4ad93f3dea380ba38 |
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| Source note | uspto-grants-2003_11 |
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