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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225946Erstellt: 26. Oktober 2026

2,6-Dichlorobenzoic acid → 2,6-Dichlorobenzoyloxymethyl ketone

https://huagongshe.com/reaction/225946

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Dichlorobenzoic acidHCID 5758—
Edukt1,3-Dibromo-2-propanoneHCID 69952—
EduktPotassium FluorideHCID 522689—
LösungsmittelDimethylformamideHCID 6228—
Produkt2,6-Dichlorobenzoyloxymethyl ketoneHCID 18517524—

Reaktionsschritte

Thus obtained bromomethyl ketone derivative (X, 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, and the mixture was stirred for two hours to give 2,6-dichlorobenzoyloxymethyl ketone derivative (XIa). This compound was dissolved in methanol (20 ml) and reacted by adding NaBH4 (412 mg)-methanol solution (40 ml)(−10□˜room temperature, two hours). The reaction was stopped by acetic acid, and the reaction solution was distilled under reduced pressure to remove methanol. The residue was extracted with ethyl acetate (50 ml×2), washed with water and aqueous sodium chloride solution, dried (anhydrous Na2SO4), concentrated under reduced pressure, and separated-purified by column chromatography (ethyl acetate-hexane, 1:5) to give the title compound (4.80 g, Yield 86%) in a diastereomeric form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557133B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-f12c119bc359443caf7f777dfcfb8f5d
Quellennotizuspto-grants-2009_07