Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | HCID 68380538 | HCID 68380538 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68380595 | HCID 68380595 | 28% |
Reaction Steps
In a 300 mL recovery flask were put 13 g (44 mmol) of N-[1-(ethylsulfanyl)isobutylidene]-4-bromoaniline, 3.9 g (29 mmol) of benzoylhydrazine, and 40 mL of 1-butanol, and the mixture was heated and refluxed at 130° C. for 10 hours. After that, 1-butanol was distilled off to give a solid. A methanol suspension of this solid was irradiated with ultrasonic waves, and a white solid was collected by gravity filtration, so that 2.8 g of white powder of 4-(4-bromophenyl)-5-isopropyl-3-phenyl-4H-1,2,4-triazole was obtained in a yield of 28%. The reaction scheme of Step 4 is shown in (b-4) below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09155158B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-5a01094a2a69470cb3aab8f5adde4919 |
|---|
| Source note | uspto-grants-2015_10 |
|---|