HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 13125206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1H-1,2,4-Triazole, 1-methyl- | HCID 22459 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13125206 | HCID 13125206 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981111B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-25cb9dfc72184c4c86bea8f3a42d3022 |
| Source note | uspto-grants-2015_03 |