The preparation method of ethyl 4-aminobenzoate powder
A technology of ethyl aminobenzoate and aminobenzoic acid, applied in the field of preparation of ethyl 4-aminobenzoate powder, can solve the problems of low production capacity, easy generation of dust, high energy consumption, etc., and achieve high production capacity and reduce pollution , the effect of low energy consumption
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Embodiment 1)
[0020] The preparation method of the ethyl 4-aminobenzoate powder of the present embodiment is as follows:
[0021] ①Add 40g of 4-nitrobenzoic acid, 200mL of water, 0.5g of 4-dimethylaminopyridine and 0.6g of 3wt% palladium carbon catalyst into the autoclave, first replace it with nitrogen three times, then feed hydrogen and adjust the pressure to 0.8±0.1MPa, and at the same time control the temperature at 100±2°C, heat preservation and pressure to complete the reaction.
[0022] After the reaction, the catalyst was recovered by filtration, the filtrate was cooled, crystallized, filtered, and dried under vacuum at 80-85°C to obtain 32.0 g of 4-aminobenzoic acid with a yield of 97.5%, a melting point of 187.0-187.5°C, and a content of 99.9 % (permanent stop titration).
[0023] ②Add 200mL of ethanol to the reaction bottle and keep the temperature at 25±5℃, then add 27g of 98wt% concentrated sulfuric acid dropwise, and then add 30g of 4-aminobenzoic acid, heat to reflux and com...
Embodiment 2)
[0041] The preparation method of the ethyl 4-aminobenzoate powder of the present embodiment is as follows:
[0042] ①Add 60g of 4-nitrobenzoic acid, 300mL of water, 1.0g of 4-dimethylaminopyridine and 1.1g of 3wt% palladium carbon catalyst into the autoclave, first replace it with nitrogen three times, then feed hydrogen and adjust the pressure to 0.8±0.1MPa, and at the same time control the temperature at 100±2°C, heat preservation and pressure to complete the reaction.
[0043] After the reaction, the catalyst was recovered by filtration, the filtrate was cooled, crystallized, filtered, and dried under vacuum at 80-85°C to obtain 47.7g of 4-aminobenzoic acid with a yield of 96.9%, a melting point of 187.1-187.6°C, and a content of 100.2 % (permanent stop titration).
[0044] ②Add 260mL of ethanol to the reaction bottle and keep the temperature at 25±5℃, then add 38g of 98wt% concentrated sulfuric acid dropwise, and then add 45g of 4-aminobenzoic acid, heat to reflux and com...
Embodiment 3)
[0049] The preparation method of the ethyl 4-aminobenzoate powder of the present embodiment is as follows:
[0050]①Add 60g of 4-nitrobenzoic acid, 300mL of water, 1.0g of 4-dimethylaminopyridine and 1.1g of 3wt% palladium carbon catalyst into the autoclave, first replace it with nitrogen three times, then feed hydrogen and adjust the pressure to 0.8±0.1MPa, and at the same time control the temperature at 100±2°C, heat preservation and pressure to complete the reaction.
[0051] After the reaction, the catalyst was recovered by filtration, the filtrate was cooled, crystallized, filtered, and dried under vacuum at 80-85°C to obtain 47.7g of 4-aminobenzoic acid, the yield was 96.9%, the melting point was 186.9-187.5°C, and the content was 99.8 % (permanent stop titration).
[0052] ② Add 260mL of ethanol to the reaction bottle and keep the temperature at 25±5°C, then add 38g of 98wt% concentrated sulfuric acid dropwise, and then add 45g of 4-aminobenzoic acid, heat to reflux an...
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