Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylhydrazine hydrochlorideHCID 60962—
ReactantN-formyl-2-phenylacetamideHCID 3268658—
SolventAcetic AcidHCID 176—
Product5-benzyl-1-phenyl-1H-1,2,4-triazoleHCID 10728463—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709469B2
Source datasetuspto-grants-2010_05
ORD IDord-e36d3b951f094df9bf03d634389e1497
Source noteuspto-grants-2010_05