Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Propionitrile | HCID 7854 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Octanenitrile | HCID 31286 | — |
| Product | 4-Methoxybenzonitrile | HCID 70129 | — |
Reaction Steps
In a Group 1 process, propanal is converted into a mixture containing some propionitrile and acrylonitrile together with acetonitrile, aldehydes, and other by-products by a reaction with gaseous ammonia and air at 460° C. over Sn/Sb oxide catalyst (M. Cathala, et al., Bull. Soc. chim. France, 1979, pp. 173-178). In another example (R. J. Card and J. L. Schmitt, J. Org. Chem., 1981, vol. 46, pp. 754-757), benzonitrile, p-methoxybenzonitrile, and octanenitrile are obtained in good yields by passing a stream of gaseous ammonia containing 5 mol % of the corresponding aldehyde through a catalyst bed (3 cm of Cu/alumina) at 325° C. According to Brit. Pat. 709,337, acrolein is converted into acrylonitrile in a gas phase reaction with air/ammonia/steam/ nitrogen mixture over molybdenum catalysts at 285-445° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06114565 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-0a37d9396aec4f1881d72fb9672e2227 |
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| Source note | uspto-grants-2000_09 |
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