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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909786Generated: October 31, 2026

5-Bromo-2-chlorobenzoic acid → HCID 67069095, compound

https://huagongshe.com/reaction/909786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 18726814HCID 18726814—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 67069095HCID 6706909570.2%

Reaction Steps

Oxalyl chloride (1.89 mL, 0.0220 mol) and N,N-dimethylformamide (0.03 mL) were added to 5-bromo-2-chlorobenzoic acid (5.0 g, 0.0212 mol) in chloroform (10 mL) and stirred for three hours. The yellow oil obtained by evaporating the solvent under reduced pressure was dissolved in chloroform (10 mL). To this solution, 2,5-difluorophenetole (3.4 g, 0.0214 mol) was added and then aluminum chloride (2.9 g, 0.0214 mol) was added portion wise at −10° C. over five minutes. After the reaction mixture was stirred at 5° C. for two hours, an iced water was added. This was extracted with chloroform three times. After the combined organic layer was washed with 1M hydrochloric acid, water, brine, it was dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain (5-bromo-2-chlorophenyl)(4-ethoxy-2,5-difluorophenyl)methanone (5.59 g, 70%) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017792B2
Source datasetuspto-grants-2011_09
ORD IDord-04cec03c3bde420c80e583dbb31dff90
Source noteuspto-grants-2011_09