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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352343Generated: November 1, 2026

Ammonia → 3-Cyanopyridine

https://huagongshe.com/reaction/2352343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3-MethylpyridineHCID 7970—
Reactant2-MethylpyridineHCID 7975—
ReactantN-MethylpiperidineHCID 12291—
Reactant3-MethylpiperidineHCID 79081—
Product3-CyanopyridineHCID 79—
Product3-MethylpyridineHCID 7970—
Product3-MethylpiperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876348
Source datasetuspto-grants-1989_10
ORD IDord-405fd59081894f29a7ea7a169b00c34a
Source noteuspto-grants-1989_10