HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Ethyl 2,2-Bis-(3-iodophenoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodophenol | HCID 12272 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2,2-Bis-(3-iodophenoxy)acetate | HCID 19959850 | 17.2% |
Reaction Steps
A stirred solution of 40.0 g (0.18 mol) of 3-iodophenol, 33.6 ml (0.18 mol) of diethyl bromomalonate and 27.63 g (0.2 moles) of milled anhydrous potassium carbonate in 250 ml dry N,N-dimethylformamide was heated at 110°-120° C. under argon for 14 hours. The mixture was cooled and concentrated in vacuo. The resulting residue was combined with 600 ml of ice-cold water and the oily product was extracted with ethyl acetate (4×150 ml). The combined ethyl acetate extracts were dried (MgSO4) and concentrated in vacuo to an orange oil. The orange oil was purified by chromatography (eluted by 5% methylene chloride in hexanes to 50% methylene chloride in hexanes) to yield 8.1 g (8.5%) of the desired product as a tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620677 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-aba6f21e242c4e97988ea0ec9c79dcb5 |
| Source note | uspto-grants-1997_04 |