39475-55-3Relevant articles and documents
Chlorpyrifos production method
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Paragraph 0033-0050, (2018/05/01)
Provided is a chlorpyrifos production method. Trichloro-acetic chloride is used as a starting raw material, an intermediate 3,3,5,6-tetrachloro-4,5-dihydropyridine-2(3H)-ketone is synthesized throughaddition and cyclization reaction, and then chlorpyrifos is synthesized through alkaline hydrolysis, condensation reaction and one-pot process reaction. The 3,5,6-trichloropyridine-2-sodium phenolatefiltering link after alkaline hydrolysis reaction is omitted, the chlorpyrifos is synthesized through a one-pot process, and operation steps are simplified. A dual-solvent method is adopted for condensation reaction, hydrolysis of O,O-diethyl thiophosphoryl chloride and generation of sulfotep can be effectively inhibited, the content of the synthesized chlorpyrifos product is 97% or above, and thetotal yield is 83% or above. Produced wastewater is greatly decreased, the total wastewater discharging amount is reduced by about 50% compared with an existing process, and the chlorpyrifos production method is suitable for industrial production.
Reinvestigation of phase-transfer-catalyzed chlorpyrifos synthesis
Fakhraian,Moghimi,Ghadiri,Dehnavi,Sadeghi
, p. 680 - 684 (2013/09/02)
Production of chlorpyrifos via the phase-transfer-catalyzed reaction of 0,0-diethylphosphorochloridothioate and the sodium salt of 3,5,6- trichloropyridin-2-ol was reinvestigated. The formation of sulfotep (the major byproduct) and the yield are influence
Fungicidal active compound combinations
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, (2008/06/13)
The present application relates to new active compound combinations composed, on the one hand, of prior art compounds metaconazole, 5-[(4-chlorophenyl)methyl]-2,2-dimethyl-1-(1H-1,2,4-triazol-1-yl-methyl)cyclopentanol and imidacloprid, 1-[(6-chloro-3-pyridinyl)-methyl]-4,5-dihydro-N-nitro-1H-imidazole-2-amine, and, on the other hand, of other prior-art active compounds, the combinations being extremely suitable for the protection of wood products.