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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064714Generated: October 26, 2026

Iodine → (4-Fluorophenyl)(4-hydroxy-3-iodophenyl)methanone

https://huagongshe.com/reaction/1064714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
Reactant4-Fluoro-4'-hydroxybenzophenoneHCID 117666—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
Product(4-Fluorophenyl)(4-hydroxy-3-iodophenyl)methanoneHCID 1138227574%

Reaction Conditions

Temperature25 °C

Reaction Steps

(4-Fluorophenyl)(4-hydroxyphenyl)methanone (20.0 g, 92.5 mmol) in concentrated ammonium hydroxide (770 mL) was allowed to stir at 25° C. for 15 minutes and then treated with potassium iodide (74.79 g, 450.5 mmol) and iodine (23.48 g, 92.5 mmol) in water (185 mL). The reaction mixture was allowed to stir at 25° C. for 18 hours and then filtered. The precipitate was dissolved in ethyl acetate, washed with water and brine, dried, filtered and the filtrate concentrated under reduced pressure to provide the title compound as a pale green solid (23.4 g, 74% yield). 1HNMR (300 MHZ, CD3OD) δ 6.91 (d, 1H, J=8.9 Hz), 7.26 (t, 2H), 7.64 (d, 1H, J=8.9 Hz), 7.78 (t, 2H), 8.17 (s, 1H); MS (DCI) m/z 342.9 (M+H)+, 360 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-ae05c85ae5e2421bbeec138a09a09540
Source noteuspto-grants-2005_11