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ChemicalBook CAS DataBase List Tebuconazole

Tebuconazole synthesis

3synthesis methods
-

Yield:107534-96-3 96.5%

Reaction Conditions:

with 3-(bromomethyl)-1-(4-chlorophenyl)-4,4-dimethylpentan-3-ol;potassium hydroxide in N,N-dimethyl-formamide at 150; for 4 h;Reagent/catalyst;Solvent;Temperature;

Steps:

1

250 ml three-mouth bottle adding N, N - dimethyl formamide 120g, and add tebuconazole isomer 40g, potassium hydroxide 2.0g, 3 - bromomethyl -1 - (4 - chlorophenyl) - 4, 4 - dimethyl -3 - propanol 1.0g. The temperature to 150 °C reaction 4h. Sampling, the measured tebuconazole 99.8%, isomer 0.2%. After the desolvation, water and toluene after pulping, filtered to obtain product tebuconazole 38.6g, yield 96.5%, content of 98.5%.

References:

CN106699675,2017,A Location in patent:Paragraph 0024-0026

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