Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | HCID 58068048 | HCID 58068048 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 58240203 | HCID 58240203 | 24% |
Reaction Steps
First, 6.1 g of N-[1-(ethylsulfanyl)isobutylidene]aniline, 3.4 g of benzoylhydrazine, and 30 mL of 1-butanol were put in a 200 mL recovery flask, and heated and stirred at 130° C. for 7 hours to be reacted. After the reaction, 1-butanol was distilled off under a reduced pressure to give an oily substance. This oily substance was purified by silica gel column chromatography. As developing solvents, first, dichloromethane was used, and then ethyl acetate was used. The resulting fraction was concentrated to give a white solid. The given solid was recrystallized from a mixed solvent of ethanol and hexane, so that 1.6 g of 3-isopropyl-4,5-diphenyl-4H-1,2,4-triazole was prepared as a white solid with a yield of 24%. The synthetic scheme of Step 1 is shown by (a-8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09065061B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-7e297d9f24f64cf1a3eefea1ac11af16 |
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| Source note | uspto-grants-2015_06 |
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