HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20231523, compound → HCID 20231522, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20231523 | HCID 20231523 | — |
| Reactant | HCID 56630335 | HCID 56630335 | — |
| Reactant | HCID 56635899 | HCID 56635899 | — |
| Product | HCID 20231522 | HCID 20231522 | 90.3% |
Reaction Steps
If there are used in the manner described under (a), instead of 250 g (1 mol) of 3,12-diisopropyl-1,2-diaza-1,5,9-cyclododecatriene, 328.5 g (1 mol) of 3,12-dicyclohexyl-1,2-diaza-1,5,9-cyclododecatriene (diastereoisomeric mixture) and correspondingly reduced amounts of catalyst and solvent, with otherwise the same procedure, there is obtained, as the main fraction, 304 g (90% of theory) of 1,10-diamino-1,10-dicyclohexyldecane in the form of colourless oil [b.p. 190°-193° C./0.05 Torr; nD20 =1.4944; IR (liquid) inter alia bands at 3355, 3278 and 1613 cm-1 ].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225701 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-b68483005575479385d76c6ca37b919f |
| Source note | uspto-grants-1980_09 |