Synthetic method for aryl thioether compounds
A technology of thiol compounds and aryl sulfides, which is applied in the field of synthesis of oxygen and nitrogen compounds, can solve the problems of high cost, reduce waste liquid, be easy to operate, and improve efficiency
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Embodiment 1
[0028] The preparation method of aryl sulfide compound is as follows:
[0029]
[0030] Add β-naphthol compound (0.5mmol), p-cresylthiol (1.5mmol), sulfonated cobalt phthalocyanine (0.025mmol) in the dry 25mL Schlenk reaction tube, add water 2mL, flush into oxygen, heat to reflux, After reacting for 18 hours, after the reaction, extract with ethyl acetate, dry the extract with anhydrous sodium sulfate, concentrate under reduced pressure to remove the solvent, and separate by column chromatography to obtain the target product.
Embodiment 2
[0032] The preparation method of aryl sulfide compound is as follows:
[0033]
[0034] Add β-naphthol compound (0.5mmol), o-bromothiophenol (83.5mg, 1.5mmol) and copper tetracarboxyphthalocyanine (0.025mmol) to the dry 25mL Schlenk reaction tube, add water 2mL, flush into oxygen, Heat to reflux and react for 24 hours. After the reaction, extract with ethyl acetate, dry the extract with anhydrous sodium sulfate, concentrate under reduced pressure to remove the solvent, and separate by column chromatography to obtain the target product.
Embodiment 3
[0036] The preparation method of aryl sulfide compound is as follows:
[0037]
[0038] Add 6-bromo-2-naphthol compound (0.5mmol), hexanethiol (1.5mmol), sulfonated iron phthalocyanine (0.025mmol) into a dry 25mL Schlenk reaction tube, add 2mL of water, flush into oxygen, and heat Return to reflux and react for 24 hours. After the reaction, extract with ethyl acetate, dry the extract with anhydrous sodium sulfate, concentrate under reduced pressure to remove the solvent, and separate by column chromatography to obtain the target product.
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