Method for preparing p-bromoanisole by oxidative bromination method
A technology of bromoanisole and oxidative bromination, applied in chemical instruments and methods, preparation of organic compounds, physical/chemical process catalysts, etc., can solve problems such as long reaction time, lengthy and complicated process, expensive precious metal palladium, etc. , to achieve high activity and selectivity, simple process flow and simple preparation process
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Embodiment example 1
[0016] Add 1.009g (12mmol) dicyandiamide to 20ml and dissolve 2.88g (1mmol) H 3 PW 12 O 40 .nH 2 60 ℃ hot water solution of O, add 1 g of activated carbon under constant stirring, stir vigorously at 60 ℃ for 5 h, after sufficient reaction, after the reaction mixture is cooled, the solvent is removed by rotary evaporation, and then the obtained solid sample is placed in a tubular Under the nitrogen atmosphere of the furnace, the calcination temperature was 350 °C, the heating rate was 5 °C / min, the temperature was maintained for 3 h, and the catalyst was naturally cooled to room temperature to obtain catalyst A1, wherein the content of PW was 45.9% (45.17%W, 0.73%P).
Embodiment example 2
[0018] Add 1.009g (12mmol) dicyandiamide to 20ml and dissolve 2.88g (1mmol) H 3 PW 12 O 40 .nH 2 60 ℃ hot water solution of O, add 1 g of activated carbon under constant stirring, stir vigorously at 60 ℃ for 5 h, after sufficient reaction, after the reaction mixture is cooled, the solvent is removed by rotary evaporation, and then the obtained solid sample is placed in a tubular Under the nitrogen atmosphere of the furnace, the calcination temperature was 450°C, the heating rate was 5°C / min, the temperature was maintained for 3 hours, and the catalyst was naturally cooled to room temperature to obtain catalyst A2, wherein the content of PW was 46.26% (45.53%W, 0.73%P).
Embodiment example 3
[0020] Add 1.009g (12mmol) dicyandiamide to 20ml and dissolve 2.88g (1mmol) H 3 PW 12 O 40 .nH 2 60 ℃ hot water solution of O, add 1 g of activated carbon under constant stirring, stir vigorously at 60 ℃ for 5 h, after sufficient reaction, after the reaction mixture is cooled, the solvent is removed by rotary evaporation, and then the obtained solid sample is placed in a tubular Under the nitrogen atmosphere of the furnace, the calcination temperature was 550°C, the heating rate was 5°C / min, the temperature was maintained for 3h, and then cooled to room temperature naturally to obtain catalyst A3, wherein the content of PW was 46.5% (45.76%W, 0.74%P).
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