HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12403257, compound → HCID 12403258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12403257 | HCID 12403257 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 12403258 | HCID 12403258 | 91.4% |
Reaction Steps
6.50 g of N,N-bis(3-(N,N-bis(2-cyanoethyl)amino)propyl)benzylamine, 0.65 g of Raney Co and 100 mL of 1,4-dioxane were charged in an autoclave and a hydrogenation reaction was carried out at an initial hydrogen pressure of 9.0 MPa at 180° C. for 2 hours. After the catalyst was removed by filtration, the obtained filtrate was concentrated to dryness to give 6.16 g of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076478B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-1af1576068644447b7aa5d8104849d5c |
| Source note | uspto-grants-2011_12 |