HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511022Generated: November 1, 2026
N-Iodosuccinimide → HCID 86666943, compound
https://huagongshe.com/reaction/511022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4'',5''-DICHLORO-2''-HYDROXYACETOPHENONE | HCID 13850167 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86666943 | HCID 86666943 | 46.1% |
Reaction Steps
A solution of 1-(4,5-dichloro-2-hydroxyphenyl)ethanone (12 g, 59 mmol) in acetic acid (70 mL) was treated with N-iodosuccinimide (16 g, 71 mmol) and stirred at 90° C. for 18 hours. The reaction mixture was treated with additional N-iodosuccinimide (8 g, 36 mmol) and stirred at 90° C. for 4 hours. The reaction mixture was concentrated, diluted with EtOAc, and quenched with saturated sodium bicarbonate until the bubbling stopped. The organic layer was separated and the aqueous phase was re-extracted with EtOAc. The combined organic layers were dried and concentrated to give a brown solid. This material was recrystallized from methanol to give desired product (9.0 g, 46%) as a tan solid. LCMS for C8H6Cl2IO2 (M+H)+: m/z=330.9, 332.9. Found: 330.8, 332.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096600B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-6db47102e71c49408876507ce9169387 |
|---|
| Source note | uspto-grants-2015_08 |
|---|