Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,3-Diaminopentane | HCID 102444 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 19877141 | HCID 19877141 | 94% |
Reaction Steps
Ninety grams (96.8% purity, 0.854 mole) 1,3-diaminopentane, 60 g acetonitrile (1.46 moles) and 3 g powdered nickel on alumina catalyst were charged to a 300 ml autoclave described in Example 1. The mixture was stirred and heated at 90° C. and 650 psig pressure for 6 hours followed by cooling to 25° C. Analysis of the filtered product on a capillary GC column showed a 42.9% conversion of 1,3-diaminopentane and 94% yield of 2-methyl-4-ethylhexahydropyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05149809 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-92394855677c42d7b78263182f86a71d |
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| Source note | uspto-grants-1992_09 |
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