HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 564838Erstellt: 25. Oktober 2026
4-Methoxyphenol → Methyl 3,5-dinitro-4-(4-methoxyphenoxy)-benzoate
https://huagongshe.com/reaction/564838
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Methoxyphenol | HCID 9015 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Methyl 4-chloro-3,5-dinitrobenzoate | HCID 96161 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 3,5-dinitro-4-(4-methoxyphenoxy)-benzoate | HCID 9819693 | 65,6% |
Reaktionsschritte
To a 100 ml round-bottomed flask containing potassium hydroxide (4.7 g; 82.0 mmol) dissolved in water (20 ml) was successively added 4-methoxyphenol (10.0 g; 80.6 mmol) and methyl 4-chloro-3,5-dinitrobenzoate (20.2 g; 77.5 mmol). The flask was fitted with a reflux condenser and the reaction heated at 150° C. (oil bath) for 3 hours. After cooling to room temp, the reaction mixture was transferred to a large mortar and triturated with cold 2N NaOH (100 ml) to remove unreacted phenol. The solid was collected by filtration and air-dried to give 21.5 g of crude product. Crystallization from absolute ethanol gave 17.7 g (65.6%) of pure methyl 3,5-dinitro-4-(4-methoxyphenoxy)benzoate as light yellow needles. 300 MHz 1H NMR (CDCl3) d 3.77 (s, 3H, OCH3), 4.02 (s, 3H, OCH3), 6.82 (m, 4H, ArH), 8.70 (s, 2H, ArH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06169104A |
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| Quelldatensatz | uspto-grants-2001_01 |
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| ORD ID | ord-dbd37e4eeec946bb917c348fb12ef5ff |
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| Quellennotiz | uspto-grants-2001_01 |
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