HuagongsheHuagongshe Chemistry Print Report · For research reference only
n,n-Bis(2-cyanoethyl)hexylamine → n,n-Bis(3-aminopropyl)hexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | n,n-Bis(2-cyanoethyl)hexylamine | HCID 16733110 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | n,n-Bis(3-aminopropyl)hexylamine | HCID 16733236 | 100.6% |
Reaction Steps
31.0 g of N,N-bis(2-cyanoethyl)hexylamine, 4.65 g of RaneyCo, 150 ml of 1,4-dioxane was charged to an autoclave, and hydrogen addition reaction was carried out by supplying hydrogen at an initial pressure of 9.1 MPa at 110° C. for 2 hours. After removing a catalyst by filtration, the obtained filtrate was concentrated and dried to obtain 32.4 g of a target compound as a pale red oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08830811B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7e8ee36758c7485db6b2a8f14bebde0b |
| Source note | uspto-grants-2014_09 |