Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lactonitrile | HCID 6572 | — |
| Reactant | 2,3-Butanediamine | HCID 136362 | — |
| Product | 84688-49-3 | HCID 13125044 | 72% |
Reaction Steps
138.5 g (1.95 moles) of acetaldehyde cyanohydrin were added dropwise to a solution of 176 g (2 moles) of 2,3-diaminobutane in 250 ml of water, with cooling at 25° C. The mixture was then heated at the boil for 8 hours, until no more ammonia was split off. The reaction mixture was then distilled under reduced pressure to give 200 g (72% of theory) of 2,5,6-trimethyl-3-oxo-piperazine of boiling point 123° C./0.5 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04636246 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-1f47e5c4f86c4ebfa3dad6257027a204 |
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| Source note | uspto-grants-1987_01 |
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