HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51629Generated: October 27, 2026
Water → Methyl-2-fluoro-4-iodo-phenyl acetate
https://huagongshe.com/reaction/51629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(2-Fluoro-4-iodophenyl)acetonitrile | HCID 22240532 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl-2-fluoro-4-iodo-phenyl acetate | HCID 69548383 | 80% |
Reaction Steps
A solution of 2-fluoro-4-iodo-phenyl acetonitrile (Intermediate 2, 3 g, 11.45 mmol) in methanol (50 mL) and benzene (50 mL) was treated with p-toluene sulfonic acid (2.5 g, 13.15 mmol) 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 6% ethyl acetate in hexane as the eluent to afford the title compound as a colorless oil (2.7 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06713647B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-98c6ba50893842a3911dc2aae50869db |
|---|
| Source note | uspto-grants-2004_03 |
|---|