Synthesis method for 4,4'-biphenyldicarboxylic acid
A biphenyl dicarboxylic acid and synthesis method technology, applied in the field of synthesis of 4,4'-biphenyl dicarboxylic acid, can solve the problems of harsh reaction conditions, numerous synthesis steps, difficult separation and purification, etc., and achieve mild process reaction conditions, process The process is reasonable and feasible, and the effect of atom economy is high
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Embodiment 1
[0018] A kind of synthetic method of 4,4'-biphenyl dicarboxylic acid, its reaction steps are as follows:
[0019] Step 1: Under the protection of nitrogen, add 53.5g (0.270mol) of 4-biphenylcarboxylic acid, 45g (0.337mol) of anhydrous aluminum trichloride and dichloroethane (solvent ) 250g, cool down to 15°C, add 41.2g (0.325mol) of oxalyl chloride dropwise, and the dropwise addition is completed within 2 hours. The hydrogen chloride gas generated during the dropwise addition is absorbed with lye. After layering in 800g of ice water, the oil layer was washed twice with water, and the solvent was recovered to obtain 60.3g of 4,4′-dicarboxybiphenylil, with a purity of 95% and a yield of 94.2%;
[0020] Step 2: In a 500ml four-necked glass reaction flask, add 60.3g (0.134mol) of 4,4′-dicarboxybiphenyl, 10.6g (0.188mol) of potassium hydroxide and 300g of dichlorobenzene (organic solvent) in sequence , control the temperature in the reaction bottle at 40-50°C and add 20.7g (0.161m...
Embodiment 2
[0022] A kind of synthetic method of 4,4'-biphenyl dicarboxylic acid, its reaction steps are as follows:
[0023] Step 1: Under the protection of nitrogen, add 53.5g (0.270mol) of 4-biphenylcarboxylic acid, 64.5g (0.484mol) of anhydrous aluminum trichloride and chloroform (solvent) into a 500ml dry four-necked reaction flask in sequence 350g, temperature controlled to 25°C, 55g (0.433mol) of oxalyl chloride was added dropwise, and the dropwise addition was completed within 2 hours, and the hydrogen chloride gas generated during the dropwise addition was absorbed with lye. After the reaction was completed, the material was slowly added to 1000g of ice water. After the layers were separated, the oil layer was washed twice with water, and the solvent was recovered to obtain 59g of 4,4'-dicarboxybiphenylil, with a purity of 96% and a yield of 93.2%. ;
[0024] Step 2: In a 500ml four-necked glass reaction flask, add 59g (0.131mol) of 4,4′-dicarboxybiphenyl, 14.6g (0.260mol) of po...
Embodiment 3
[0026] A kind of synthetic method of 4,4'-biphenyl dicarboxylic acid, its reaction steps are as follows:
[0027] Step 1: Under nitrogen protection, add 53.5g (0.270mol) of 4-biphenylcarboxylic acid, 57.8g (0.433mol) of anhydrous aluminum trichloride and dichloroethane (solvent ) 350g, the temperature was controlled to 20°C, 48g (0.378mol) of oxalyl chloride was added dropwise, and the dropwise addition was completed within 2 hours, and the hydrogen chloride gas generated during the dropwise addition was absorbed with lye. After the reaction was completed, the material was slowly added to 1000g of ice water. After the layers were separated, the oil layer was washed twice with water, and the solvent was recovered to obtain 60g of 4,4'-dicarboxybiphenylil, with a purity of 96% and a yield of 94.7%. ;
[0028] Step 2: In a 500ml four-necked glass reaction flask, add 60g (0.133mol) of 4,4′-dicarboxybiphenyl, 13.5g (0.241mol) of potassium hydroxide and 400g of chlorobenzene (organ...
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