HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Diethyl 4-cyanobenzylacetamidomalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Diethylacetamidomalonate | HCID 21751412 | — |
| Product | Diethyl 4-cyanobenzylacetamidomalonate | HCID 33254412 | 91% |
Reaction Steps
Suspend diethylacetamidomalonate (44 g, 0.203 mol), alpha-bromo-p-toluonitrile (40 g, 0.204 mol), potassium iodide (10 g) in dioxane (400 mL) and add a solution of sodium ethoxide (4.6 g of sodium in 200 mL of dry ethanol). Heat under reflux the mixture for 3-4 hours and let stay overnight. Pour the mixture on ice (2 L), filtrate the precipitate, wash with water and dry on lyophyliser. Recrystallize from methanol, to give diethyl 4-cyanobenzylacetamidomalonate as white crystals (61 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05766932 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-337318d7450b453fad4e23045aaf1595 |
| Source note | uspto-grants-1998_06 |