HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N,N-Bis(3-aminopropyl)dodecylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Dodecylamine | HCID 13583 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-Bis(3-aminopropyl)dodecylamine | HCID 75407 | 373.1% |
Reaction Steps
670 g of laurylamine (C12 -fraction: 73 mole %, and C14 -fraction: 23 mole %) were reacted in the manner already described in Example 1 with 373 g of acrylonitrile in 68 g of water, 34 g of methanol and 14 g of concentrated acetic acid, and the product was then hydrogenated. 2,020 g of bis-(3-aminopropyl)-laurylamine were obtained after the hydrogenation. 954 g of this triamine were condensed with 640 g of ethylene oxide. 1,590 g of bis-(3-aminopropyl)-laurylamine ethoxylate (99%) were obtained. 257 g of this ethoxylate and 538 g of water were reacted with 146 g of 70% by weight strength H2O2. The triamine-trioxide was obtained in 935 g of a 30% by weight strength aqueous solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415488 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-0298ce8dc1774378b454b153852d1766 |
| Source note | uspto-grants-1983_11 |