HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexadecylamine → N-(2-hydroxyethoxy)ethyl-n-hexadecylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexadecylamine | HCID 8926 | — |
| Reactant | 2-(Chloroethoxy)ethanol | HCID 12361 | — |
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-hydroxyethoxy)ethyl-n-hexadecylamine | HCID 9996690 | 70% |
Reaction Steps
Into a 1 l rounded-flask, were introduced 48.2 g of hexadecyl amine and 700 ml of ethanol. The mixture was heated to reflux, and then was gradually added 11 ml of 2-(2-chloroethoxy)ethanol. The mixture was refluxed for 3 hours and cooled to a room temperature. Thereto was added solution of KOH/ethanol to produce precipitates, which were removed by filtration. The filtrate was concentrated under reduced pressure, and then was recrystallized from ethanol, and dried to give 24.1 g of the title compound(Yield: 70%) as white powder, which was identified by IR and NMR. The results are shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06060612 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-7b93908ad6e64715811b802693a3f15e |
| Source note | uspto-grants-2000_05 |