HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Ethyl 4-ethoxy-3-iodobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-hydroxy-3-iodobenzoate | HCID 11220038 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 4-ethoxy-3-iodobenzoate | HCID 44829074 | — |
Reaction Steps
To the resultant ester (3.10 g, 10.61 mmol) and potassium carbonate (2.87 g, 20.75 mmol) in 40 ml acetonitrile, add iodoethane (1.3 ml, 16.25 mmol) at RT while stirring vigorously. Heat the resulting white suspension under reflux for 1.5 h. Evaporate acetonitrile and replace with EtOAc. Wash the organic layer first with water, then with saturated aq. sodium chloride. Dry over anhydrous sodium sulfate, filter and concentrate to give the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393868B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-e0e2f0eb362345f4b8af51323376579c |
| Source note | uspto-grants-2008_07 |