Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| 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 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, 100 g (0.38 mol) of xylene were added and the reaction mixture was stirred for 21 hours at a temperature of 150° C. Amount of 2-fluoronitrobenzene formed, according to GC analysis:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05476976 |
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| Quelldatensatz | uspto-grants-1995_12 |
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| ORD ID | ord-465347a2c41342d48226a5bbf0083f9d |
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| Quellennotiz | uspto-grants-1995_12 |
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