HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819555Generated: November 2, 2026
Potassium Iodide → 1-(2-Hydroxy-5-iodophenyl)ethan-1-one
https://huagongshe.com/reaction/1819555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(5-Amino-2-hydroxyphenyl)ethanone | HCID 2775222 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-(2-Hydroxy-5-iodophenyl)ethan-1-one | HCID 42636728 | 39% |
Reaction Steps
To a stirring solution of 1-(5-amino-2-hydroxy-phenyl)-ethanone (6.856 g,46 mmol) in 98% sulfuric acid (24 ml) and water (19 ml) was added sodium nitrite (3.30 g, 48 mmol, 1.05 equ) in water (5.5 ml). The reaction was stirred for 35 minutes, then sulfuric acid (4 ml), copper powder (0.17 g, 0.3 mmol, 0.06 equ) and potassium iodide (8.80 g, 53 mmol, 1.16 equ) in water (5.5 ml) added. The mixture was then heated slowly to 65° C. and maintained at 65° C. for 2 hours. The reaction was then cooled, water (25 ml) and sodium hydrogen carbonate added. More water was added, then extracted into a mixture of ethyl acetate and dichloromethane, then ethyl acetate (2×). The combined organic layers were washed with brine then concentrated in vacuo. This mixture was then taken up in ethyl acetate and 2 M HCl, filtered and the organic layer dried (MgSO4) and concentrated in vacuo to give 1-(5-iodo-2-hydroxy-phenyl)-ethanone 52 (1.339 g, 39%) as a purple oil. This was then used in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07601754B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-b89564d7530e4e97b1355f765cbbd9e2 |
|---|
| Source note | uspto-grants-2009_10 |
|---|