Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | N-Iodosuccinimide | HCID 120273 | — |
| Edukt | 3-Chloro-4-fluoroanisole | HCID 2773585 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Chloro-2-fluoro-4-iodo-5-methoxybenzene | HCID 21070630 | 70,4% |
Reaktionsschritte
A round-bottom flask was charged with 2-chloro-1-fluoro-4-methoxybenzene (Alfa Aesar, Ward Hill, Mass., 2.714 g, 16.90 mmol), DCM (24.86 ml), AcOH (24.86 ml), and sulfuric acid (0.496 ml, 9.30 mmol) to give a solution. n-iodosuccinimide (3.80 g, 16.90 mmol) was added in a single portion. TLC showed what appeared to be conversion of the starting material to a slightly higher, move UV-active spot. The mixture was diluted with DCM, washed with water (2×), washed with saturated aq. sodium thiosulfate, dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (50-g SNAP Ultra column, 0-10% EtOAc/Heptane) to give 3.409 g of a clear oil. This oil was used directly in the next reaction without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09012443B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-0323f11afe314e979ec1f231d4171d33 |
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| Quellennotiz | uspto-grants-2015_04 |
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