HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,6-Di(propan-2-yl)benzene-1,3-diamine → HCID 14573497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,6-Di(propan-2-yl)benzene-1,3-diamine | HCID 12702128 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14573497 | HCID 14573497 | 28% |
Reaction Steps
A suitable autoclave was charged with 20.7 g (0.108 mol) of purified 1,3-diamino-4,6-diisopropylbenzene, 0.3 g (2.7 mmol) of potassium t-butoxide, 2.0 g of 5% Ru on alumina, and 100 mL of t-butanol. The autoclave was heated to 190° C. at 25.5 MPa hydrogen for 24 hours. It was then cooled and its contents filtered. The solvent was removed from the filtrate in vacuo and the resulting liquid distilled through a 20.3 cm Vigreaux column at about 4 mm Hg/115°-118° C. to give 5.9 g (28%) of 1,3-diamino-4,6-diisopropylcyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04849544 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-9ef92ffbc1fc414087c0bfcf379009cc |
| Source note | uspto-grants-1989_07 |