<div>A new series of substituted anthranilic esters derivatives linked with a 1,3-dithiolane and</div><div>benzyloximino moiety was synthesized using the simple esterfication reaction and products were</div><div>fully characterized. The isolated yields of these compounds range from 59 to 96%. 1,3-</div><div>dithiolane ester and the benzyloxy substituted diamine derivatives are white solids and stable to</div><div>air and moisture. The synthesized compounds can be exhibits UV-vis absorption properties by</div><div>their structures with a amine or amide group, It is observed that absorption maximum is excellent</div><div>for 2,6-disubstituted benzyloxy esters which can be explained by electron transfer or conjugation</div><div>is steric effect in ortho substitution from the amino group and the amide group.</div>

<div>A new series of substituted anthranilic esters derivatives linked with a 1,3-dithiolane and</div><div>benzyloximino moiety was synthesized using the simple esterfication reaction and products were</div><div>fully characterized. The isolated yields of these compounds range from 59 to 96%. 1,3-</div><div>dithiolane ester and the benzyloxy substituted diamine derivatives are white solids and stable to</div><div>air and moisture. The synthesized compounds can be exhibits UV-vis absorption properties by</div><div>their structures with a amine or amide group, It is observed that absorption maximum is excellent</div><div>for 2,6-disubstituted benzyloxy esters which can be explained by electron transfer or conjugation</div><div>is steric effect in ortho substitution from the amino group and the amide group.</div>

<p>We report the synthesis of new aromatic derivatives containing the 1,3-dithiolane ether and benzyloximino moiety which are attached by simple alkylation and esterification reaction by treating 1,3-dithiolane-2-methanol and a-benzyloximino acid chloride respectively with various aromatic halides and alcohols, respectively. The isolated yields of these compounds range from 65 to 85%. 1,3-dithiolane ether and the benzyloxy substituted hydroquinone are white solids or residual oil and stable to air and moisture. </p>

<p>We report the synthesis of new aromatic derivatives containing the 1,3-dithiolane ether and benzyloximino moiety which are attached by simple alkylation and esterification reaction by treating 1,3-dithiolane-2-methanol and a-benzyloximino acid chloride respectively with various aromatic halides and alcohols, respectively. The isolated yields of these compounds range from 65 to 85%. 1,3-dithiolane ether and the benzyloxy substituted hydroquinone are white solids or residual oil and stable to air and moisture. </p>

A new series of substituted anthranilic esters derivatives linked with a 1,3-dithiolane and benzyloximino moiety was synthesized using the simple esterfication reaction and products were fully characterized. The isolated yields of these compounds range from 59 to 96%. 1,3dithiolane ester and the benzyloxy substituted diamine derivatives are white solids and stable to air and moisture. The synthesized compounds can be exhibits UV-vis absorption properties by their structures with a amine or amide group, It is observed that absorption maximum is excellent for 2,6-disubstituted benzyloxy esters which can be explained by electron transfer or conjugation is steric effect in ortho substitution from the amino group and the amide group.