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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446896Erstellt: 24. Oktober 2026

2,6-Dichlorobenzoic acid → 2,6-Dichlorobenzoxymethylketone

https://huagongshe.com/de/reaction/446896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Dichlorobenzoic acidHCID 5758—
Edukt1,3-Dibromo-2-propanoneHCID 69952—
EduktPotassium FluorideHCID 522689—
LösungsmittelDimethylformamideHCID 6228—
Produkt2,6-DichlorobenzoxymethylketoneHCID 57116688—

Reaktionsschritte

The bromomethylketone derivative (4.36 g) and 2,6-dichlorobenzoic acid (2.28 g, 1.1 eq) were dissolved in dimethylformamide (18 mL), KF (1.58 g, 2.5 eq) was added thereto, and the mixture was stirred for 2 h at room temperature. The residue obtained by concentration under reduced pressure was extracted with ethyl acetate, washed with water, twice with saturated aqueous sodium hydrogen carbonate solution, and aqueous sodium chloride solution, dried (anhydrous Na2SO4), and concentrated under reduced pressure to give the 2,6-dichlorobenzoxymethylketone derivative. This compound was dissolved in methanol (20 mL), and reacted by adding NaBH4 (412 mg)-methanol solution (40 mL). The reaction mixture was slowly warmed to room temperature for 2 h. The reaction was stopped by acetic acid. The reaction mixture was distilled under reduced pressure to remove methanol, extracted with ethyl acetate (50 mL×2), washed with water and aqueous sodium chloride solution, dried (anhydrous Na2SO4), concentrated under reduced pressure, and separated by column chromatography (ethyl acetate-hexane, 1:5) to give 4.80 g (86%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481537B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-1c66c55cd3054a8987ea98100c12c731
Quellennotizuspto-grants-2013_07