Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-Methylpyridine | HCID 7970 | — |
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | 3-Methylpiperidine | HCID 79081 | — |
| Product | 3-Cyanopyridine | HCID 79 | — |
| Product | 3-Methylpyridine | HCID 7970 | — |
| Product | 3-Methylpiperidine | HCID 79081 | — |
Reaction Steps
2.0 cc of the 80% PV3MO12Ox.20% SiO2 catalyst of Example 2 was placed in the microreactor and equilibrated at 405° C., then a gaseous mixture containing 7.5 moles of NH3 and 19.9 moles of air for each mole of the mixed heterocyclic containing 0.82 mole of 3-methylpyridine and 0.18 mole of 3-methylpiperidine was fed through the reactor using a contact time of 6.4 seconds. Conversion of the methylpiperidine was 100 percent and conversion of the methylpyridine was 92 percent. For each mole of combined 3-methylpiperidine plus 3-methylpyridine fed was obtained 0.853 mole of 3-cyanopyridine. If it be assumed that all of the converted 3-methylpyridine formed 3-cyanopyridine, the minimum selectivity of 3-methylpiperidine to 3-cyanopyridine was 50 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04876348 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-405fd59081894f29a7ea7a169b00c34a |
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| Source note | uspto-grants-1989_10 |
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