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HRID 446896作成日:2026年10月26日

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

https://huagongshe.com/reaction/446896

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dichlorobenzoic acidHCID 5758—
反応物1,3-Dibromo-2-propanoneHCID 69952—
反応物Potassium FluorideHCID 522689—
溶媒DimethylformamideHCID 6228—
生成物2,6-DichlorobenzoxymethylketoneHCID 57116688—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481537B2
出典データセットuspto-grants-2013_07
ORD IDord-1c66c55cd3054a8987ea98100c12c731
出典メモuspto-grants-2013_07