A kind of synthetic method of v-type rigid flexible molecule based on pyrene and multi-branched polyethylene glycol chain
A technology of polyethylene glycol and synthesis method, applied in chemical instruments and methods, preparation of organic compounds, organic chemistry, etc., can solve problems such as unclear influence, achieve high fluorescence quantum efficiency, high yield, and improve solubility Effect
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Embodiment 1
[0039] 1) Synthesis of intermediate 2a
[0040]
[0041] Dissolve 0.83g (4.5mmol) of methyl gallate and 3.13g (22.7mmol) of anhydrous potassium carbonate in 50mL of refined acetonitrile, then weigh 4.96g (18.1mmol) of compound a, and dissolve it with 15mL of refined acetonitrile Dissolved, poured into a constant pressure funnel and slowly added dropwise to the above solution, the dropwise addition continued for about 1.5 hours, and the ice bath device was removed after the dropwise addition, and refluxed for 24 hours. After cooling, the solvent was spinned out, washed with water, extracted three times with dichloromethane, dried, filtered, concentrated, separated and purified by column chromatography (ethyl acetate and dichloromethane with a mass ratio of 1:20 were used as eluent) to obtain Yellow oil compound 2a weighed 1.8 g, and the yield was 70%. 1H-NMR (400MHz, CDCl 3 )δ7.26(s,2H),4.18(s,6H),3.81(d,9H),3.69(s,6H),3.52(d,6H),3.35(d,9H).
[0042] 2) Synthesis of Inter...
Embodiment 2
[0054] 1) Synthesis of intermediate 2b
[0055]
[0056] Dissolve 0.74g (4.46mmol) of methyl 3,5-dihydroxybenzoate and 3.1g (22.9mmol) of anhydrous potassium carbonate in 60mL of refined acetonitrile, then weigh a 4.97g (11.04mmol), and refine with 20mL Dissolve it in acetonitrile, pour it into a constant pressure dropping funnel and slowly add it dropwise to the above solution, and reflux for 20 hours. After cooling, the solvent was spinned out, washed with water, extracted three times with dichloromethane, dried, filtered, concentrated, separated and purified by column chromatography, and the eluent was methanol:dichloromethane=1:30 (v / v), to obtain 2.91 g of light yellow oil compound 2b, yield 90.1%. 1H-NMR (400MHz, CDCl 3 )δ7.18(s,2H),6.69(s,1H),4.13(d,4H),3.92-3.80(m,8H),3.69(d,12H),3.54(s,4H),3.37(s ,6H).
[0057] 2) Synthesis of intermediate 3b
[0058]
[0059] 2b (1.5g, 2.07mmol) was dissolved in 30mL of refined methanol, potassium hydroxide (1.16g, 20.7mmo...
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