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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethoxyphenolHCID 9015—
EduktPotassium HydroxideHCID 14797—
EduktMethyl 4-chloro-3,5-dinitrobenzoateHCID 96161—
LösungsmittelWaterHCID 962—
ProduktMethyl 3,5-dinitro-4-(4-methoxyphenoxy)-benzoateHCID 981969365,6%

Reaktionsbedingungen

Temperatur150 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06169104A
Quelldatensatzuspto-grants-2001_01
ORD IDord-dbd37e4eeec946bb917c348fb12ef5ff
Quellennotizuspto-grants-2001_01