Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Adiponitrile | HCID 8128 | — |
| Reactant | Silica | HCID 24261 | — |
| Reactant | Calciumoxide | HCID 6850728 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Iron | HCID 23925 | — |
| Catalyst | HCID 178419084 | HCID 178419084 | — |
| Product | 1,2-Diaminocyclohexane | HCID 4610 | — |
| Product | Hexamethylenediamine | HCID 16402 | 98.22% |
Reaction Steps
DE-A-2 429 293 discloses in Example 1 that the hydrogenation of adiponitrile in the presence of five times the weight of ammonia at from 93 to 98° C. (inlet temperature into the reactor) or at from 94 to 104° C. (outlet temperature) over an iron catalyst prepared from magnetite by reduction with hydrogen and doped with aluminum oxide, silicon dioxide, calcium oxide and vanadium pentoxide yields 98.22% of hexamethylenediamine comprising 1900 ppm of 1,2-diaminocyclohexane, and in Example 2 that the hydrogenation of adiponitrile in the presence of five times the weight of ammonia at from 93 to 98° C. (inlet temperature into the reactor) or at from 94 to 104° C. (outlet temperature) over an iron catalyst prepared from Labrador hematite ore (Fe2O3) by reduction with hydrogen and doped with aluminum oxide, silicon dioxide and calcium oxide yields 98.05% of hexamethylenediamine comprising 3500 ppm of 1,2-diaminocyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852669B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-c8b6d278b0a24cc8912200c5841b5d1b |
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| Source note | uspto-grants-2005_02 |
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