A novel racemic chiral organic boron nitrogen fluorescent compound and its preparation method
A fluorescent compound and a racemization technology are applied in the field of novel quinoline chiral organic boron nitrogen compounds and their preparation, which can solve the problems of unreported synthesis of chiral quinoline boron nitrogen compounds and the like.
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preparation example 1
[0025] Add 0.1 mmol I (where Rf=CF3; R3, R4, R5=H), 0.1 mmol II (where R1, R2, R6=H), 0.005 mmol CuI, 0.1 mmol R7COOH (R7=Ph) into a 10 mL reaction tube and 1mL touluene, under a nitrogen atmosphere, the reaction was carried out at 150°C for 12h. After the reaction was completed, it was filtered, concentrated, and separated by chromatography to obtain III (wherein Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7 =Ph), the productive rate is 81%. Detection of catalytic activity: add 0.5mmol aniline (Ar=Ph), 0.5mmol benzaldehyde (Ar=Ph), 0.6mmol4-phenylcyclohexanone, 0.002mmol III (wherein Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7=Ph) and 1mL toluene, the reaction was carried out at 80°C for 12h, followed by TLC until the reaction was complete. The reaction result was: (E )-2-benzyl-4-phenylcyclohexanone, the productive rate is 95%, the selectivity of (E)-2-benzyl-4-phenylcyclohexanone is 100%, and the cis-trans selectivity is 1 / 99.
preparation example 2
[0027] Add 0.1 mmol I (where Rf=CF3; R3, R4, R5=H), 0.1 mmol II (where R1, R2, R6=H), 0.005 mmol KI, 0.1 mmol R7COOH (R7=Ph) into a 10 mL reaction tube and 1mL touluene, under a nitrogen atmosphere, the reaction was carried out at 150°C for 12h. After the reaction was completed, it was filtered, concentrated, and separated by chromatography to obtain III (wherein Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7 =Ph), the yield is 83%. Detection of catalytic activity: add 0.5mmol aniline (Ar=Ph), 0.5mmol benzaldehyde (Ar=Ph), 0.6mmol4-methoxycyclohexanone, 0.002 mmol III (wherein Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7=Ph) and 1mL toluene, the reaction was carried out at 80°C for 12h, and the reaction was followed by TLC until the reaction was complete. The reaction result was: ( E)-2-benzyl-4-methoxycyclohexanone, the productive rate is 97%, the selectivity of (E)-2-benzyl-4-methoxycyclohexanone is 100%, cis-trans selection Sex is 1 / 99.
preparation example 3
[0029]Add 0.1mmol I (where Rf=CF3; R3, R4, R5=H), 0.1mmol II (where R1, R2, R6=H), 0.005mmol LiI, 0.1mmol R7COOH (R7=Ph) into a 10mL reaction tube and 1mL touluene, under a nitrogen atmosphere, the reaction was carried out at 150°C for 12h. After the reaction was completed, it was filtered, concentrated, and separated by chromatography to obtain III (wherein Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7 =Ph), the productive rate is 84%. Detection of catalytic activity: add 0.5mmol aniline (Ar=Ph), 0.5mmol benzaldehyde (Ar=Ph), 0.6mmol4-trifluoromethylcyclohexanone, 0.002mmol III (where Rf=CF3; R1, R2, R3, R4, R5, R6=H, R7=Ph) and 1mL toluene, the reaction was carried out at 80°C for 12h, followed by TLC until the reaction was complete. The reaction result was: (E)-2-benzyl-4-trifluoromethylcyclohexanone, the productive rate is 91%, the selectivity of (E)-2-benzyl-4-trifluoromethylcyclohexanone is 100%, The cis-trans selectivity is 1 / 99.
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