Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Catalyst | Tetraethylammonium Iodide | HCID 6225 | — |
| Product | N,N-Dibenzylethanolamine | HCID 22657 | 83% |
Reaction Steps
0.5 gram of dibenzylamine (2.5 mmol), 0.446 gram of ethylenecarbonate (5 mmol) and 0.215 gram of tetraethylammoniumiodide (083 mmol) were mixed together at room temperature. The solid mixture was then heated at 140° C. and the resulting suspension was stirred at this temperature for 26 hours. The reaction mixture was diluted with ethyl acetate and extracted with 10 mL of a 0.5M solution of sodium hydroxide. The aqueous phase was washed with ethyl acetate and the combined organic phases were washed twice with brine. The organic phase was dried on magnesium sulfate, filtered, concentrated under reduced pressure and purified by flash chromatography on silica gel (eluant: ethylacetate/hexane 1/2) to afford 0.5 gram of N,N-dibenzyl-2-aminoethanol (yield: 83%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08338490B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-17d712ab46c84f61b8a0255fae1776b8 |
|---|
| Source note | uspto-grants-2012_12 |
|---|