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ChemicalBook CAS DataBase List Lactofen
77501-63-4

Lactofen synthesis

1synthesis methods
Lactofen is commercially produced via a 4–5 step convergent synthesis that begins with nitration of 4-chlorobenzotrifluoride to 4-chloro-3-nitrobenzotrifluoride using an acid mixture, followed by nucleophilic aromatic substitution with ethyl 2-hydroxypropionate under basic conditions to form the diphenyl ether linkage. Reduction of the nitro group to amine is achieved via catalytic hydrogenation. The key acylation uses 2-chloro-4-(trifluoromethyl)phenoxyacetyl chloride in the presence of triethylamine in dichloromethane.
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Yield:-

Reaction Conditions:

with potassium hydroxide in ethyl acetate;Heating;Solvent;Reagent/catalyst;

Steps:

1

In a 5000 ml four-necked reaction flask equipped with azeotropic dehydration apparatus, 2,500 ml of ethyl acetate solvent was added and stirredStirring and then into the acifluorfen 1000g (2.76 mol), 170 g (3.0 moles) of potassium hydroxide as a sheet, and 440 g (3.22 moles) of ethyl 2-chloropropionate were added. After completion of the heating, the reaction-produced water was removed by azeotropic dehydration. In 80 ~ 85 ° C insulation, while the reaction side of the system dehydration, to be completely reacted acifluorfen, the vacuum of -0.095MPa, the liquid temperature f 80 ° C ethyl acetate evaporated, and finally through (60 ~ 80 ° C). The purity of the product was 88.3% and the yield was 98.2%. The purity of the product was 88.3%.

References:

CN103694123,2016,B Location in patent:Paragraph 0024-0027

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