Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4,4-Dimethyl-5-oxohexanenitrile | HCID 13157782 | — |
| Reactant | 2,3,3-Trimethylpiperidine | HCID 19005191 | — |
| Catalyst | Titanium oxide (Ti3O) | HCID 162651 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | 4,4-Dimethyl-1,5-hexanediamine | HCID 18314354 | 93% |
Reaction Steps
10 g of 4,4,-dimethyl-5-oxohexanenitrile (purity 97.2%) and 195 g of liquid ammonia were pumped hourly from bottom to top at 250 bar and 80° C. through a tubular reactor (diameter 16 mm, fill level 50 cm, oil-heated twin jacket) arranged before the hydrogenation reactor and filled with 63.5 g (100 ml) of titanium dioxide (anatase) in the form of 1.5 mm pellets. 100 l (s.t.p.)/h of hydrogen were subsequently passed in, and the product discharged from the upstream imination reactor was passed through the hydrogenation reactor from bottom to top at 250 bar and 110° C. The mixture was decompressed to atmospheric pressure, the ammonia was removed by distillation, and the hydrogenation product was analyzed quantitatively by means of gas chromatography, giving a yield of 93.0% of 4,4-dimethyl-1,5-hexanediamine and 4.5% of 2,3,3-trimethylpiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344983 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-7bcfdf88c3ee4646af86ea7d7bde11eb |
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| Source note | uspto-grants-1994_09 |
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