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ChemicalBook CAS DataBase List Pyraclostrobin
175013-18-0

Pyraclostrobin synthesis

7synthesis methods
Production involves a multi-step synthesis starting with p-chlorophenylhydrazine hydrochloride and ortho-nitrotoluene as key raw materials. The process includes sequential reactions such as synthesis, cyclization, oxidation, bromination, etherification, reduction, esterification, and methylation to build the final strobilurin structure. One efficient method uses methyl [2-(bromomethyl)phenyl]methoxycarbamate and 1-(4-chlorophenyl)-3-hydroxy-1H-pyrazole in the presence of potassium carbonate and acetone under reflux conditions for several hours. After filtration, drying, and crystallization, the final product is obtained with high purity and yield, making the process suitable for industrial-scale production.
151827-83-7 Synthesis
Methyl [2-(bromomethyl)phenyl]methoxycarbamate

151827-83-7
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76205-19-1 Synthesis
1-(4-CHLOROPHENYL)-3-HYDROXY-1H-PYRAZOLE

76205-19-1
202 suppliers
$7.00/5g

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Yield:175013-18-0 83%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide;propan-2-one; for 7 h;Reflux;

Steps:

2.5 Example 2

(5) Dissolving methyl N-methoxy-N- (2-bromomethylphenyl) carbamate with DMF as solvent0.12 mol of 1- (4-chlorophenyl) -pyrazolol, 0.15 mol of K2CO3 and acetone were placed in a reactor. After the temperature was raised to reflux, a solution of 0.1 mol of N-methoxy-N-2-bromomethylphenylcarbamate solution was refluxed for 7 hours. After filtration and drying, the solid material was completely dissolved by stirring with anhydrous methanol, and then cooled and crystallized to obtain a light The yellow solid is the target product pyraclostrobin.
The purity of the product pyraclostrobin prepared by the above method was 89.1% and the yield was 83%

References:

CN106008347,2016,A Location in patent:Paragraph 0027; 0033; 0034

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