Added Abstract w/o percent yields and all

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@@ -44,10 +44,18 @@ from Commerical Asprin Tablets to Form Methyl Salicylate}
\maketitle
\begin{abstract}
This is an example document for creating \LaTeX{} submissions to the American
Chemical Society (ACS) for publication. As ACS does not use \LaTeX{} for
typesetting accepted manuscripts, this template does not seek to
reproduce the appearance of a published paper.
Methyl salicylate was synthesized from commercial aspirin tablets via an acid-catalyzed
tandem hydrolysisesterification sequence. Acetylsalicylic acid (ASA) was extracted
from the tablet matrix into methanol and reacted under reflux with a catalytic
volume of \ce{H2SO4}. This one-pot method facilitates simultaneous deacetylation
and Fischer esterification, bypassing the isolation of a salicylic acid intermediate.
The resulting methyl salicylate was isolated via aqueous quenching and
liquid--liquid extraction. Crude product purification was achieved through
neutralization with saturated \ce{NaHCO3} and drying over anhydrous \ce{MgSO4}.
This synthesis demonstrates an efficient, high-yield conversion of a common
pharmaceutical precursor into a high-value fragrance ester, highlighting
fundamental principles of equilibrium-driven organic transformations and
multistep one-pot synthesis.
\end{abstract}