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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1810855Erstellt: 25. Oktober 2026

Nitric Acid → 5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl ester

https://huagongshe.com/reaction/1810855

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
Eduktm-Chlorophenethylic alcoholHCID 78856—
EduktMethyl 3-hydroxy-4-methoxybenzoateHCID 4056967—
Edukt3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076296—
Produkt5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl esterHCID 67076791—

Reaktionsschritte

Methyl 3-hydroxy-4-methoxybenzoate and 2-(3-chlorophenyl)-ethanol were reacted in analogy to step 1 of example 1. The obtained 3-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester (0.750 g, 2.34 mmol) was added slowly to ice-cooled 100% nitric acid (10 ml). The ice bath was removed and stirring was continued overnight. The mixture was cautiously transferred into a stirred mixture of EA, water and an excess of sodium hydrogencarbonate and extracted with EA. The combined organic extracts were washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The solid residue was extracted with diethyl ether, and the ethereal solution was evaporated. The residue was stirred with HEP, and the solid was filtered and dried in vacuo to give 0.680 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08362073B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-eba5bcc5c160423cbeda28b09a845051
Quellennotizuspto-grants-2013_01