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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330718Generated: October 25, 2026

3-Chlorobenzoic Acid → HCID 58019514, compound

https://huagongshe.com/reaction/330718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzoic AcidHCID 447—
ReactantWaterHCID 962—
ReactantDibenzo(f,h)quinoxalineHCID 252644—
SolventDichloromethaneHCID 6344—
ProductHCID 58019514HCID 5801951451%

Reaction Steps

First, to a solution in which 1.36 g of dibenzo[f,h]quinoxaline was dissolved in 20 mL of dichloromethane was added 2.04 g of 3-chlorobenzoic acid (abbreviation: MCPBA) in a nitrogen atmosphere, followed by stirring at room temperature for 1 week. Water was added to this mixture, and the organic layer was extracted with dichloromethane. The obtained organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate. Then, the resulting solution was filtered. The solvent of this solution was distilled off. The resulting residue was purified by silica gel column chromatography which uses a mixed solvent of dichloromethane and ethyl acetate as a developing layer. By recrystallization from dichloromethane, the object of the synthesis was obtained (as a white powder in a yield of 51%). The synthesis scheme of Step 1 is illustrated in the following (a″′-2-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877351B2
Source datasetuspto-grants-2014_11
ORD IDord-c39679544a5f462f8753084078463a6e
Source noteuspto-grants-2014_11