Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 2-Naphthohydrazide | HCID 123485 | — |
| Reactant | HCID 58068048 | HCID 58068048 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58240205 | HCID 58240205 | 37% |
Reaction Steps
First, 5.7 g of N-[1-(ethylsulfanyl)isobutylidene]aniline, 4.4 g of 2-naphthohydrazide, and 40 mL of 1-butanol were put in a 100 mL three-neck flask, and heated and stirred at 120° C. for 20 hours to be reacted. After the reaction, 1-butanol was distilled off to give a brown oily substance. Toluene was added to this oily substance, whereby a solid was precipitated, and then filtrated to give the solid. The resulting solid was recrystallized from toluene, so that 2.7 g of 3-isopropyl-5-(2-naphthyl)-4-phenyl-4H-1,2,4-triazole (abbreviation: HiPrntz) was prepared as a white solid with a yield of 37%. The synthetic scheme of Step 1 is shown by (a-13). As described above, the objective compound of Example 14 has a favorable yield.
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-b5523514ca3241eea2eca83f077df617 |
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| Source note | uspto-grants-2015_06 |
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