HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232971Generated: October 30, 2026
Triethylamine → 5-benzyl-1-phenyl-1H-1,2,4-triazole
https://huagongshe.com/reaction/2232971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Reactant | N-formyl-2-phenylacetamide | HCID 3268658 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-benzyl-1-phenyl-1H-1,2,4-triazole | HCID 10728463 | — |
Reaction Steps
Phenylhydrazine hydrochloride (0.09 g, 0.6 mmol) in 5 mL glacial acetic acid was treated with triethylamine (0.06 g, 0.6 mmol), warmed to 70° C., treated with N-formylphenylacetamide (0.1 g, 0.6 mmol), and heated at 90° C. for 1 hour. The mixture was then allowed to cool to room temperature and was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the organics were washed with saturated NaHCO3, 1M NaOH, water, and brine. The organics were then dried (MgSO4), and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (40% hexanes/ethyl acetate) to provide the title compound. MS (ESI) m/e: 236 (M+H)+; 1H NMR (DMSO-d6) δ 4.2 (s, 2H), 7.05-7.1 (d, 2H), 7.17-7.3 (m, 3H), 7.45-7.6 (m, 5H), 8.1 (s, 1H); Anal. calcd. for C, 76.57; H, 5.57; N, 17.86. Found C, 76.32; H: 5.81; N, 17.63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709469B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-e36d3b951f094df9bf03d634389e1497 |
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| Source note | uspto-grants-2010_05 |
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