HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Acrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methane | HCID 297 | — |
| Reactant | Ethane | HCID 6324 | — |
| Reactant | Propane | HCID 6334 | — |
| Reactant | Isobutane | HCID 6360 | — |
| Reactant | Butane | HCID 7843 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Acrylonitrile | HCID 7855 | — |
| Product | Methacrylonitrile | HCID 31368 | — |
Reaction Steps
The reaction used in the present invention is a gas phase catalytic oxidation reaction of an alkane with ammonia, i.e. an ammoxidation reaction of an alkane. As the alkane, methane, ethane, propane, n-butane, isobutane, pentane, hexane, heptane, or cyclohexane may, for example, be mentioned. Taking the industrial application of the resulting nitrile into consideration, however, it is preferred to employ a C1-4 alkane, particularly propane and/or butane, from a viewpoint such that as the resulting nitrile, acrylonitrile and/or methacrylonitrile can be obtained in good yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534650 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-a01d6f40f5ed41238c0e28c0cdbc75dc |
| Source note | uspto-grants-1996_07 |