Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-(Trifluoromethyl)phenyl isocyanate | HCID 73768 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 135480553 | HCID 135480553 | 78% |
Reaction Steps
To 4-trifluoromethylphenyl isocyanate (2.89 ml, 20.2. mmol) was added 5.36 ml of azidotrimethylsilane (39.9 mmol), and the mixture was stirred at 110° C. for twenty-four hours. After cooling, the mixture was subjected to column chromatography using silicagel (eluate; ethyl acetate:hexane=1;1 to 2:1 to ethyl acetate) to collect a desired fraction to be concentrated. The crystals obtained were recrystallized from ethyl acetate-hexane to give 3.64 g of 1-(4-trifluoromethylphenyl)-5(1H,4H)-tetrazolone (78%) as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466820 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-d17e46b177d9415c839c41b7348a2bdb |
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| Source note | uspto-grants-1995_11 |
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