HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 5'-Chloro-2'-hydroxy-4'-methylacetophenone | HCID 598229 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone | HCID 11472394 | — |
Reaction Steps
To a stirred solution of 1-(5-chloro-2-hydroxy-4-methylphenyl)ethanone (20 g, 110 mmol) in acetic acid (200 mL) was added N-iodosuccinimide (29 g, 130 mmol) and the resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo, neutralized with saturated sodium bicarbonate, filtered off insoluble succinimide and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude product was recrystallized from a mixture of ethyl acetate and hexane (25.8 mg, 77%). LCMS calculated for C9H9ClIO2 (M+H)+: m/z=311.0. found: 311.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096600B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9ca9c602a3cc4166a7dfb78be86487eb |
| Source note | uspto-grants-2015_08 |