HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Diethyl 2-(2,4,6-Triiodophenoxy)-1,3-propanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Triiodophenol | HCID 11862 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-(2,4,6-Triiodophenoxy)-1,3-propanedioate | HCID 15343336 | 64% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A stirred mixture of 70.8 g (0.15 mol) of 2,4,6-triiodophenol, 39.0 g (0.15 mol) of diethyl bromomalonate and 20.7 g (0.15 mol) of milled anhydrous potassium carbonate in 200 ml of dry dimethylformamide was heated at 100° C. under argon for 5 hours. The mixture was cooled and concentrated in vacuo. The resulting residue was combined with 300 ml of ice-cold water and the oily product was extracted with ethyl acetate (1×300 ml), 3×100 ml). The combined ethyl acetate extracts were dried (MgSO4) and concentrated in vacuo to a dark oil. The oil was purified by chromatography (eluted by hexanes to 20% diethyl ether in hexanes) to yield 60.2 g (64%) of product as a light cream-colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05316755 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-1f97a3d33be443deb93bf70c83f23c58 |
| Source note | uspto-grants-1994_05 |