HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-(N,N-dibenzylglycyl)-o-anisamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-((Bis(benzyl)amino)acetyl)salicylamide | HCID 121727 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5-(N,N-dibenzylglycyl)-o-anisamide | HCID 20318584 | — |
Reaction Steps
5-(N,N-Dibenzylglycyl)salicylamide (37.4 g) was heated at reflux for 2 hours with methyl iodide (10 ml) and anhydrous potassium carbonate (20 g) in ethyl methyl ketone (350 ml). The inorganic salts were filtered off and the solvent was evaporated in vacuo. The residue was dissolved in ethyl acetate, washed with water and again evaporated. The residual oil was crystallised from isopropanol to give 5-(N,N-dibenzylglycyl)-o-anisamide as a white solid, (14 g) m.p. 113°-114° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101579 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-3dbfaee30a5140ceba3423c1666c732f |
| Source note | uspto-grants-1978_07 |