HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-Cyanopyridine
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 80% PV3MO12Ox.20% SiO2 catalyst of Example 1 was placed in the microreactor and equilibrated at 405° C., then a gaseous mixture of 0.82 3-methylpyridine:0.18 3-methylpiperidine:7.5 NH3 :19.9 air 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 93 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 |
|---|---|
| Patent number | US04603207 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-7289a97e319c4625b3a0466d2c88ecf1 |
| Source note | uspto-grants-1986_07 |