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ChemicalBook CAS DataBase List Diflubenzuron
35367-38-5

Diflubenzuron synthesis

10synthesis methods
The commercial production of diflubenzuron begins with the synthesis of the active ingredient through the reaction of 2,6-difluorobenzamide with 4-chlorophenyl isocyanate, typically catalysed by dimethylformamide in a controlled solvent environment to form N-[[(4-chlorophenyl)amino]carbonyl]-2,6-difluorobenzamide. The reaction mixture is then purified via filtration, extraction, and recrystallisation to achieve high purity while minimising impurities like 4-chloroaniline.
-

Yield:-

Reaction Conditions:

in 5,5-dimethyl-1,3-cyclohexadiene at 140; for 5 h;Large scale;Temperature;

Steps:

1-7 Example 1 of the present invention provides a synthesis process of diflubenzuron

Specifically: 576Kg of aromatic hydrocarbon solvent xylene is measured and then injected into the condensation reactor, Then add 157Kg 2,6-difluorobenzamide, The temperature was raised to 140°C and refluxed for 4h. After finishing, Cool down to 40 and start adding 148.7Kg p-chlorophenyl isocyanate dropwise, After the addition, the temperature was raised to 140°C and reacted for 5 hours. Cool down to 60, The crystal is filtered, washed with water, and dried for 8 hours to obtain the diflubenzuron product. The aromatic hydrocarbon solvent xylene is distilled and reused.

References:

CN112876384,2021,A Location in patent:Paragraph 0055-0068

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