HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → HCID 178467490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Cyclobutyl-5-(5-ethoxy-4H-1,2,4-triazol-3-yl)-2-methylbenzonitrile | HCID 178467489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178467490 | HCID 178467490 | — |
Reaction Steps
To a solution of 4-cyclobutyl-5-(5-ethoxy-4H-1,2,4-triazol-3-yl)-2-methylbenzonitrile (219.7, 0.15 g, 0.53 mmol) in EtOH (10 ml) was added NH4OH (0.18 ml, 2.66 mmol, 14.8 N in H2O) followed by H2O2 (1.8 ml, 26.6 mmol, 50% in H2O). The mixture was stirred at room temperature overnight. The mixture was cooled to 0° C. and quenched carefully with 1N Na2S2O3 solution (26 ml). The mixture was extracted with EtOAc (×2) and the combined organic layers were dried over Na2SO4, filtered, and concentrated. The residue was purified with prep-TLC (5% MeOH in CH2Cl2). Yield: 0.1 g, white solid, 62.5%. m/z (ES−) 299 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871790B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-a3e3d45d5ba840c6862017f32b55cf7a |
| Source note | uspto-grants-2014_10 |