HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ethyl 7-(2,4,6-triiodophenoxy)heptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Triiodophenol | HCID 11862 | — |
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 7-(2,4,6-triiodophenoxy)heptanoate | HCID 22939821 | 187.8% |
Reaction Steps
Dimethylformamide (DMF, 20 mL) was added with ethyl 7-bromoheptanoate (4.7 g) and 2,4,6-triiodophenol (2.4 g), further added with potassium carbonate (2.1 g) and stirred at room temperature for one day. The reaction solution was added with water and extracted twice with ethyl acetate, and the organic layer was washed three times with water and dried over anhydrous magnesium sulfate. Then, the solvent was removed, and the resulting residue was purified by silica gel column chromatography to obtain ethyl 7-(2,4,6-triiodophenoxy)heptanoate (6.0 g, yield: 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07371877B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-64d2d6a489964f28bd603479f6a4793f |
| Source note | uspto-grants-2008_05 |