Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Styrylphenylamine | HCID 13265 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 73741285 | HCID 73741285 | 324.3% |
Reaction Steps
To a 25 mL round bottom in a drybox was added nitrosonium tetrafluoroborate (0.11 g, 0.95 mmol). Acetonitrile (2 mL) was added and the flask was cooled down to −30° C. A solution of 4-STYRYLPHENYLAMINE (0.17 g, 0.86 mmol) and BHT (0.19 g, 0.86 mmol) in acetonitrile (5 mL) was added dropwise via syringe. The reaction was allowed to warm to −5° C. over 20 min. Ether (10 mL) was then added and the precipitate was filtered. The title compound was purified by re-precipitating from acetonitrile (3 mL) with ether (15 mL) to yield 0.82 g (34%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176146B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-19f7e283f2bb4b389844dbe4f9489af6 |
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| Source note | uspto-grants-2007_02 |
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