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DEVELOPMENT OF A TECHNOLOGICAL SCHEME FOR THE SYNTHESIS OF PHENYL-3-METHYLPHENOXYPROPIONATE BY REACTION OF PHENYL-2-CHLOROPROPIONATE WITH 3-METHYLPHENOL

Authors

Ochilov Mansur, Abdushukurov Anvar Kabirovich, Mamatkulov Nematillo Narzullaevich, Rajabov Shohzodbek Holmuratovich

Rubric:Chemistry
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The article presents nucleophilic substitution reactions of phenyl-2-chloropropionate with 3-methylphenol under various conditions and a method for preparing phenyl-3-methylphenoxypropionate. Nucleophilic substitution reactions were carried out in the solvents benzene, acetone, dioxane, DMF (Dimethylformamide), and DMSO (Dimethyl sulfoxide). It was found that these solvents affect the duration and yield of the reaction. In the reaction, phenyl-3-methylphenoxypropionate was obtained in a DMSO solution with a yield of 83%. A technological scheme for the synthesis of phenyl-3-methylphenoxypropionate in acetone was developed. The reason is that acetone is a cheap solvent and is convenient for the industrial production of organic substances. The structure of the synthesized new organic substance, phenyl-3-methylphenoxypropionate, was confirmed using modern IR, ¹HyAMR and 13CYaMR spectra.

Keywords

substitution
synthesis
chloroacetylation
solvent
technological scheme.
analysis
organic synthesis
reagent
extraction
3-methylphenol
nucleophile

Authors

Ochilov Mansur, Abdushukurov Anvar Kabirovich, Mamatkulov Nematillo Narzullaevich, Rajabov Shohzodbek Holmuratovich

References:

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Abdushukurov A. K., Yusufov M. S. Study of the reaction of isomeric aminophenols with chloroacetyl chloride // Universum: Technical sciences: electronic scientific journal. 2020. No. 3(72). P. 74-75. http://7universum.com/ru/tech/archive/item/9096.

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