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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390198Erstellt: 24. Oktober 2026

Phenol → 2-(Dimethoxymethyl)-1-nitro-4-phenoxybenzene

https://huagongshe.com/de/reaction/390198

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktDiisopropyl EtherHCID 7914—
EduktPotassium CarbonateHCID 11430—
Edukt4-Chloro-2-(dimethoxymethyl)-1-nitrobenzeneHCID 3570093—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2-(Dimethoxymethyl)-1-nitro-4-phenoxybenzeneHCID 3480452—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of 4-chloro-2-dimethoxymethyl-1-nitrobenzene (11.55 g, 0.0500 mol), phenol (4.70 g, 0.0500 mol), and potassium carbonate (8.16 g, 0.0600 mol) in DMA (100 mL) was stirred at 150° C. for 6 h. After cooling, the reaction mixture was poured into water and treated with diisopropyl ether. The organic layer was separated, washed with 10% aqueous KOH solution, dried (MgSO4), filtered, and concentrated. The resulting residue was purified by column chromatography on silica gel using as eluent CH2Cl2:petroleum ether (40:60, 60:40, 100:0 gradient). The product containing fractions were combined and evaporated to yield a residue which was dissolved in CH2Cl2 and washed with 10% aqueous KOH solution to remove the remaining phenol. Drying and evaporation yielded a residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383637B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-1bdecdc5e01d40cdb0b37d0f40d60b20
Quellennotizuspto-grants-2013_02