Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | 4-Methylpentane-1,2-diol | HCID 91171 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Katalysator | Tetramethylammonium chloride | HCID 6379 | — |
| Produkt | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
Reaktionsschritte
In a 2 liter flange flask and fitted with a distillation bridge and impeller stirrer, 290.5 g (5.0 mol) of potassium fluoride, 71.1 g (0.1 mol) of trimethyl(ethoxypolyoxypropyl)ammonium chloride, 11.0 g (0.1 mol) of tetramethylammonium chloride and 17.7 g (0.035 mol) of polyethylene glycol dimethyl ether 500 were introduced at 120° C. into the melt of 630 g (4.0 mol) of 2-chloronitrobenzene. Subsequently, the mixture was azeotropically dried using 100 g (0.94 mol) of xylene and the reaction mixture was stirred for 28 hours at a temperature of 150° C. Amount of 2-fluoronitrobenzene formed: after 6 hours: 36 GC area-%. after 28 hours: 74 GC area-%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05492875 |
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| Quelldatensatz | uspto-grants-1996_02 |
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| ORD ID | ord-0b691696bfe941abaf71715355a8db72 |
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| Quellennotiz | uspto-grants-1996_02 |
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