Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Nitronium tetrafluoroborate | HCID 11073463 | — |
| Reactant | HCID 178518970 | HCID 178518970 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178518974 | HCID 178518974 | 60.3% |
Reaction Steps
A solution of 1-phenyl-5-tetrazolone (30 g) in acetonitrile (300 mL) was stirred under argon at 0° C. and nitronium tetrafluoroborate (36.9 g) was added over 30 minutes. After stirring at 0° C. for an additional 30 minutes the mixture was poured into water (900 mL). The precipitate was collected by filtration and dried under vacuum to give 23.1 g of the title compound as cream-colored solids. The filtrate was extracted with ethyl acetate, dried (MgSO4), filtered, and concentrated to give an additional 8.6 g of solids which was a 1:1 mixture of ortho- and para-substituted isomers. 1H NMR (acetone-d6) δ 13.62 (br s, 1 H), 8.36 (ABq, JAB =9.2 Hz, 4 H); MS (EI) m/z 207 (M+); Rf=0.2 (10% methanol/dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051586 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-8f77b9d854f54177a68bc0457957669b |
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| Source note | uspto-grants-2000_04 |
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