HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494818Generated: October 25, 2026
Iodine → (4-Fluorophenyl)(4-hydroxy-3-iodophenyl)methanone
https://huagongshe.com/reaction/494818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Fluoro-4'-hydroxybenzophenone | HCID 117666 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | (4-Fluorophenyl)(4-hydroxy-3-iodophenyl)methanone | HCID 11382275 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07538138B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-0da99411b31348cc993256a8b9a5432c |
|---|
| Source note | uspto-grants-2009_05 |
|---|