Epoxy curing agent Knowledge Preparation and application of 1-(4-methoxyphenyl)-1,2,2-tristyrene_Kain Industrial Additive

Preparation and application of 1-(4-methoxyphenyl)-1,2,2-tristyrene_Kain Industrial Additive

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Background and overview[1]

After hydrolysis of 1-(4-methoxyphenyl)-1,2,2-tristyrene, the intermediate 1-(4-hydroxyphenyl)-1,2,2-tristyrene can be prepared. The intermediate can be used to synthesize tetrastyrene Schiff base red light zinc ion probe to effectively detect atypical metal ions.

Preparation[1]

Dissolve diphenylmethane (12mmol, 2.02g) in 50ml tetrahydrofuran, at minus 20°C, under nitrogen protection, add dropwise 2.5M n-butyllithium (10mmol, 4ml), and then add dropwise 4-methoxybis Benzophenone (12mmol, 3.03g) was heated to room temperature, stirred for 3 hours, quenched with water, extracted with dichloromethane, spin off the solvent, added toluene, p-toluenesulfonic acid (1.8mmol, 0.342g), refluxed for 6 hours, and cooled At room temperature, wash twice with 5% sodium bicarbonate aqueous solution, dry over anhydrous magnesium sulfate, spin off the solvent, and obtain a yellow crude product, which is recrystallized to obtain a white solid product compound 1-(4-methoxyphenyl)-1,2. 2-Tristyrene, yield 80%. 1HNMR (400MHz, DMSO-d6) δ (TMS, ppm): 7.19-7.06 (m, 9H), 7.03-6.92 (m, 6H), 6.87 (d, J=8.7Hz, 2H), 6.70 (d, J=8.8Hz, 2H), 3.67 (s, 3H).

Apply[1]

The intermediate 1-(4-hydroxyphenyl)-1,2,2-tristyrene can be prepared after hydrolysis of 1-(4-methoxyphenyl)-1,2,2-tristyrene. To synthesize tetrastyrene Schiff base red light zinc ion probe, the specific reaction steps are as follows: Compound 1-(4-methoxyphenyl)-1,2,2-tristyrene (4.4mmol, 1.72g) is dissolved in Glacial acetic acid, add 48% hydrobromic acid (50ml), reflux and stir for 12 hours, evaporate the solvent, add toluene and re-evaporate, extract with ethyl acetate, wash twice with sodium bicarbonate and saturated brine, and dry over anhydrous magnesium sulfate , spin off the solvent, and perform column chromatography (n-hexane/ethyl acetate = 10:1) to obtain the product 1-(4-hydroxyphenyl)-1,2,2-tristyrene. 1HNMR (400MHz, CDCl3)δ (TMS, ppm) 7.16–7.10 (m, 9H), 7.08–7.02 (m, 6H), 6.92 (d, J=8.3Hz, 2H), 6.59 (d, J=8.3Hz, 2H), 4.61 (s, 1H).

References

[1]CN201710135796.5 tetrastyrene Schiff base red light zinc ion probe and its preparation method and use

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