Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 19475 | HCID 19475 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | p-Tolunitrile | HCID 7724 | — |
Reaction Steps
In a flask p-xylene (1 ml), t-butyl nitrite (1 mmol), N-hydroxyphthalimide (0.1 mmol), and acetic acid (1 ml) were placed and were stirred at 80° C. in an atmosphere of argon gas (1 atm=0.101 MPa) for 20 hours. The resulting reaction mixture was analyzed to find that p-methylbenzaldehyde oxime, p-methylbenzaldehyde, and p-methylbenzonitrile were formed in yields of 55%, 4%, and 5%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06768023B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-dd65ae7a6c0d45e3a68fb96c78b5e11e |
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| Source note | uspto-grants-2004_07 |
|---|