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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928677Generated: October 31, 2026

2,3-Dichloropropene → HCID 90384249, compound

https://huagongshe.com/reaction/928677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 50999469HCID 50999469—
SolventAcetoneHCID 180—
ProductHCID 90384249HCID 9038424975%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Bromo-4,5-difluorothiophenol (4.68 g, 20.8 mmol), 2,3-dichloro-1-propene (2.1 mL, 22.9 mmol), potassium carbonate (3.45 g, 24.9 mmol), and acetone (100 mL) were added, and stirred at 60° C. for 2 hours. The solvent was distilled away under reduced pressure, and after diluted with ethyl acetate, the resultant was washed with water and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was distilled away, and to the resulting residue, dimethylaniline (50 mL) was added, and stirred at 220° C. overnight. After cooling, ethyl acetate and a 2 N hydrochloric acid aqueous solution were added to the reaction solution and stirred. After the insoluble material was filtered off, extraction was performed with ethyl acetate. The organic phase was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane) to thus obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290487B2
Source datasetuspto-grants-2016_03
ORD IDord-9896ef128abd4c309f89dbb38819bb55
Source noteuspto-grants-2016_03