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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856948Generated: October 31, 2026

Dimethylformamide → HCID 53865887, compound

https://huagongshe.com/reaction/1856948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 54283810HCID 54283810—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 53865887HCID 5386588774.2%

Reaction Steps

To a solution of 2-[(3-methyl-4-methoxyphenyl)methylene]-6-hydroxy-3(2H)-benzofuranone 0.477 g, potassium carbonate 0.583 g and dimethylformamide 5 ml, methyl p-toluenesulfonate 0.314 g was added. After the mixture was stirred for two hours at a temperature of 60° C., water 100 ml was added. The resulting compound was extracted with ethyl acetate 50 ml twice. The ethyl acetate solution was washed with a saturated sodium chloride solution 50 ml twice, dehydrated with anhydrous magnesium sulfate, and concentrated at a temperature of 40° C. under reduced pressure to obtain crude powder. The residue was fractionated by silica gel column chromatography (silica gel: 50 g, eluted with solvent 500 ml of hexane:ethyl acetate=1:1) and the fraction was concentrated to dryness at a temperature of 40° C. under reduced pressure to obtain crystals. The crystals were dissolved in ethyl acetate 2 ml and hexane 10 ml, and the solution was allowed to stand at room temperature for two hours. The precipitated crystals were filtered and dried over phosphorous pentoxide at a temperature of 60° C. for four hours under reduced pressure to obtain the desired compound 371.6 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143779
Source datasetuspto-grants-2000_11
ORD IDord-d28b258b3fce4c308fa1896b0f555bbf
Source noteuspto-grants-2000_11