Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dihexylamine | HCID 8920 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-fluoro-N,N-di-n-hexyl-4-nitroaniline | HCID 90024145 | 86% |
Reaktionsschritte
To a solution of 3,4-difluoronitrobenzene (1.59 g, 10 mmol) in DMSO (15 mL) were added K2CO3 (3.04 g, 22 mmol) and di-n-hexylamine (2.04 g, 11 mmol). The mixture was heated at 90° C. overnight, then cooled to rt, diluted with water (50 mL) and extracted with CH2Cl2 (50 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/CH2Cl2 (V/V)=10:1) to give the title compound as pale yellow oil (2.79 g, 86%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434695B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-ba52dcdca5224e56bb6328da85a7e25d |
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| Quellennotiz | uspto-grants-2016_09 |
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