HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332569Erstellt: 26. Oktober 2026
Hydrochloric Acid → 1-Fluoro-2-(4-fluoro-phenoxy)-3-Methoxy benzene
https://huagongshe.com/reaction/332569
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | N,N-Dimethylglycine | HCID 673 | — |
| Edukt | 4-Fluoroiodobenzene | HCID 9605 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 2-Fluoro-6-methoxyphenol | HCID 2737367 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 1-Fluoro-2-(4-fluoro-phenoxy)-3-Methoxy benzene | HCID 57701118 | 6.350,2% |
Reaktionsschritte
To a suspension of 2-fluoro-6-methoxy phenol (1) (2.8 g, 20 mmol), N,N-dimethyl glycine.HCl (837 mg, 6 mmol), Cs2CO3 (13 g, 40 mmol), 1-fluoro-4-iodobenzene (2.3 mL, 20 mmol), in Dioxane (40 ml) was added copper iodone (381 mg, 2 mmol). The reaction mixture was stirred at 105° C. over 1 week. Upon heating the reaction mixture turned from brown to a bright green. After cooling to room temperature, the reaction mixture was filtered and the filtrate was concentrated in-vacuo. The crude was purified by silica gel eluted with hexane/EtOAc (10:1), concentrated in-vacuo, to provide 300 g (21% yield) of product (2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08877816B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-6114c9b5157c4a06afa58a4a0bff2316 |
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| Quellennotiz | uspto-grants-2014_11 |
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