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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446896Generated: October 26, 2026

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

https://huagongshe.com/reaction/446896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzoic acidHCID 5758—
Reactant1,3-Dibromo-2-propanoneHCID 69952—
ReactantPotassium FluorideHCID 522689—
SolventDimethylformamideHCID 6228—
Product2,6-DichlorobenzoxymethylketoneHCID 57116688—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481537B2
Source datasetuspto-grants-2013_07
ORD IDord-1c66c55cd3054a8987ea98100c12c731
Source noteuspto-grants-2013_07