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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(5-Amino-2-hydroxyphenyl)ethanoneHCID 2775222—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product1-(2-Hydroxy-5-iodophenyl)ethan-1-oneHCID 4263672839%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601754B2
Source datasetuspto-grants-2009_10
ORD IDord-b89564d7530e4e97b1355f765cbbd9e2
Source noteuspto-grants-2009_10