Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | t-Butyl bromide | HCID 10485 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | 2-Nitro-4-phenoxybenzoic acid | HCID 17989326 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Tert-butyl 2-nitro-4-phenoxybenzoate | HCID 67342192 | — |
Reaktionsschritte
9.9 g of potassium carbonate, 0.82 g of benzyltriethyl-ammonium chloride and 21 mL of 2-bromo-2-methylpropane were added to 14 mL of N,N-dimethylacetamide solution containing 0.93 g of 2-nitro-4-phenoxybenzoic acid at room temperature and stirred at 55° C. for 18 hours. After the reaction mixture was cooled to room temperature, water and ethyl acetate were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium hydrogen carbonate aqueous solution, 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure to obtain 0.86 g of tert-butyl 2-nitro-4-phenoxybenzoate as white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07999132B2 |
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| Quelldatensatz | uspto-grants-2011_08 |
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| ORD ID | ord-9b0ee9658cf344ea805af8881975cceb |
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| Quellennotiz | uspto-grants-2011_08 |
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