HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395023Generated: October 29, 2026
Ethanol → Ethyl-2-fluoro-4-iodo-phenyl acetate
https://huagongshe.com/reaction/395023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(2-Fluoro-4-iodophenyl)acetic acid | HCID 22240393 | — |
| Reactant | 2-Fluoro-iodo-phenyl acetic acid | HCID 22568909 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl-2-fluoro-4-iodo-phenyl acetate | HCID 69548701 | 73% |
Reaction Steps
A solution of 2-fluoro-iodo-phenyl acetic acid (Intermediate 3, 1.75 g, 6.22 mmol) in ethanol (50 mL) and benzene (100 mL) was treated with concentrated sulfuric acid (1.4 mL) and heated at reflux overnight using a Dean-Stark water trap. The volatiles were distilled off in vacuo and the residue was diluted with water and diethyl ether. The phases were separated and the organic phase was washed with saturated aqueous sodium bicarbonate (×1), water (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 5%-10% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow solid (1.4 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06603019B2 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-88c2ae33f32f404daa495e6e6624f5b3 |
|---|
| Source note | uspto-grants-2003_08 |
|---|