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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875234Generated: October 31, 2026

Benzoyl chloride → HCID 13125206, compound

https://huagongshe.com/reaction/875234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1H-1,2,4-Triazole, 1-methyl-HCID 22459—
SolventAcetonitrileHCID 6342—
ProductHCID 13125206HCID 1312520658%

Reaction Steps

To a solution of 1-methyl-1H-1,2,4-triazole (5.0 g, 60.17 mmol, 1 eq.) in 250 ml of MeCN cooled to −5° C. were added Benzoyl chloride (8.45 g, 60.17 mmol, 1 eq.) and TEA (6.39 g, 8.8 ml, 63.18 mmol, 1.05 eq.) dropwise. Upon complete addition the temperature was raised to r.t. and the reaction stirred overnight. The white solid was removed by filtration and the solvent evaporated. The yellow residue was triturated in EtOAc and the white solid removed by filtration. The solvent was evaporated and the resulting brown solid was recrystalised in EtOAc/IPE to give (1-methyl-1H-1,2,4-triazol-5-yl)(phenyl)methanone (6.5 g, 58% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981111B2
Source datasetuspto-grants-2015_03
ORD IDord-25cb9dfc72184c4c86bea8f3a42d3022
Source noteuspto-grants-2015_03