A method for preparing fully substituted calix[8]arene phosphate derivatives
An aromatic hydrocarbon phosphate, full substitution technology, applied in chemical instruments and methods, compounds of Group 5/15 elements of the periodic table, organic chemistry, etc., can solve incomplete substitution of derivatives, complex synthetic routes, low yield, etc. problems, to achieve the effects of easy purification, simple synthetic route, and high reaction yield
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Synthetic example 1
[0019] Take 4g (3mmol) of p-tert-butylcalix[8]arene, 8.58g (60mmol) of dimethyl chlorophosphate, 0.4g of tetrabutylammonium bromide (TBAB) and 200ml of dichloromethane (DCM), and mix well with electromagnetic stirring 100ml of 50% aqueous sodium hydroxide solution was slowly dripped into the reaction system, the reaction system was heated to reflux, and the reaction process was detected by thin layer chromatography until the reaction was complete.
[0020] After the reaction was completed, the organic layer was separated, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, the residue was dissolved in methanol, precipitated with water, filtered, the filter cake was dissolved in ether and washed with water, the organic layer was dried with anhydrous sodium sulfate, and the solvent was evaporated to obtain a white solid a with a yield of 92 %, its product purity is greater than 95%.
Synthetic example 2
[0022] The synthesis method is similar to Synthesis Case 1, take 4g (3mmol) calix[8]arene, 10.32g (60mmol) diethyl chlorophosphate, 0.4g tetrabutylammonium bromide (TBAB) and 200ml dichloromethane (DCM) to add Put it into a 500ml three-neck flask, stir it evenly with electromagnetic stirring, slowly drop 100ml of 50% sodium hydroxide aqueous solution into the reaction system, raise the temperature of the reaction system to reflux, and detect the reaction progress by thin-layer chromatography until the reaction is complete. After the reaction was completed, it was washed with saturated brine and water. After purification, it was white powder b with a yield of 90%.
Synthetic example 3
[0024] The synthesis method is similar to Synthesis Case 1, take 4g (3mmol) calix[8]arene, 12g (60mmol) diethyl chlorophosphate, 0.4g tetrabutylammonium bromide (TBAB) and 200ml dichloromethane (DCM) into In a 500ml three-neck flask, electromagnetically stir and mix evenly, slowly drop 100ml of 50% sodium hydroxide aqueous solution into the reaction system, raise the temperature of the reaction system to reflux, and detect the reaction progress by thin-layer chromatography until the reaction is complete. After the reaction was completed, it was washed with saturated brine and water. After purification, it was a white powder c with a yield of 86%.
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