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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446896생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/446896

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dichlorobenzoic acidHCID 5758—
반응물1,3-Dibromo-2-propanoneHCID 69952—
반응물Potassium FluorideHCID 522689—
용매DimethylformamideHCID 6228—
생성물2,6-DichlorobenzoxymethylketoneHCID 57116688—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481537B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-1c66c55cd3054a8987ea98100c12c731
출처 메모uspto-grants-2013_07