Method for synthesizing n-acetylsulfanilyl chloride by using sulfur trioxide as sulfonating agent
A technology of acetaminobenzenesulfonyl chloride and sulfur trioxide, applied in the preparation of sulfonic acid, organic chemistry, etc., can solve the problems of additive influence, high processing cost, and waste acid, so as to ensure quality, protect the environment, and save processing cost Effect
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Embodiment 1
[0015] The present embodiment provides a method for the synthesis of acetaminobenzenesulfonyl chloride with sulfur trioxide as a sulfonating agent, which comprises the following steps:
[0016] (a) Add 13.5kg of acetanilide and 30kg of glacial acetic acid successively in the reactor, stir and heat up to 40°C;
[0017] (b) Feed sulfur trioxide gas into the reaction kettle (the flow rate of ventilation is 2.5L / min), and react at 40°C for 15 hours; when approaching the end of the reaction, sample and analyze every 15min (analyze using liquid chromatograph HPLC) , until the complete conversion of acetanilide, stop feeding sulfur trioxide gas;
[0018] (c) making the temperature in the reactor rise to 65°C, and reclaiming glacial acetic acid under reduced pressure;
[0019] (d) Control the temperature in the reactor to 60°C, add 12 kg of thionyl chloride dropwise and react for 4 hours (the tail gas is recovered with lye, such as 1mol / L sodium carbonate solution), and recover unrea...
Embodiment 2
[0021] The present embodiment provides a method for the synthesis of acetaminobenzenesulfonyl chloride with sulfur trioxide as a sulfonating agent, which comprises the following steps:
[0022] (a) Add 13.5kg of acetanilide and 60kg of glacial acetic acid successively in the reactor, and stir and heat up to 70°C;
[0023] (b) Feed sulfur trioxide gas into the reactor (the flow rate of ventilation is 13.0L / min), and react at 70°C for 3 hours; when approaching the end of the reaction, take samples for analysis every 5 minutes (analyze using liquid chromatograph HPLC) , until the complete conversion of acetanilide, stop feeding sulfur trioxide gas;
[0024] (c) making the temperature in the reactor rise to 80°C, and reclaiming glacial acetic acid under reduced pressure;
[0025] (d) Control the temperature in the reactor to 90°C, add 15 kg of thionyl chloride dropwise and react for 2 hours (the tail gas is recovered with lye, such as 1mol / L sodium carbonate solution), and recove...
Embodiment 3
[0027] The present embodiment provides a method for the synthesis of acetaminobenzenesulfonyl chloride with sulfur trioxide as a sulfonating agent, which comprises the following steps:
[0028] (a) Add 13.5kg of acetanilide and 45kg of glacial acetic acid successively in the reactor, stir and heat up to 50°C;
[0029] (b) Feed sulfur trioxide gas into the reaction kettle (the flow rate of ventilation is 8.0L / min), and react at 50°C for 5 hours; when approaching the end of the reaction, sample and analyze every 10min (analyze using liquid chromatograph HPLC) , until the complete conversion of acetanilide, stop feeding sulfur trioxide gas;
[0030] (c) making the temperature in the reactor rise to 70°C, and reclaiming glacial acetic acid under reduced pressure;
[0031] (d) Control the temperature in the reactor to 80°C, add 13 kg of thionyl chloride dropwise and react for 3 hours (the tail gas is recovered with lye, such as 1mol / L sodium carbonate solution), and recover unreac...
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