Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adiponitrile | HCID 8128 | — |
| Reactant | 1,3-Diaminopentane | HCID 102444 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 11790115 | HCID 11790115 | 59% |
Reaction Steps
Fifty grams of 1,3-diaminopentane (99%, 0.485 mole), 116 g (1.07 moles) adiponitrile and 2.3 g Raney® nickel were charged to a 300 cc autoclave reactor. The mixture was stirred and heated at 90° C. and 650 psig hydrogen pressure for 10 hours. The mixture was cooled and filtered under nitrogen. Capillary GC analysis of the filtered product indicated a 56% conversion of 1,3-diaminopentane and 59% yield of 2-(4-cyanobutyl)-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-f780b039d0d64d7ca86d84d7c92cf120 |
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| Source note | uspto-grants-1992_09 |
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