Synthesis and decarboxylation of 2,3-Dioxophenylpyrrolidine- 3-carboxylic acid etyhl ester / Julieyana Abdul Manap

Abdul Manap, Julieyana (2009) Synthesis and decarboxylation of 2,3-Dioxophenylpyrrolidine- 3-carboxylic acid etyhl ester / Julieyana Abdul Manap. [Student Project] (Unpublished)

Abstract

There were two stage involved in this experiment. The first stage was the synthesis of the 2,3-dioxopyrrolidines and second stage was decarboxylation. In the first stage of synthesis there were three reagents used to produce the ring systems. There were diethyl oxalate, anisaldehyde and an amine. Different amines used were benzylamine and methylamine. The products obtained 1-phenyl-4,5-dioxo-2-pheyl-pyrrolidine-3-carboxylic acid ethyl ester and 1-methyl-4.5-dioxo-2-phenyl-pyrrolidine-3-carboxylic acid ethyl ester respectively. The products were characterized using NMR. In decarboxylation, each product from the first stage was refluxed with 10% HCl for 5 hours and extracted with dichloromethane and ethyl acetate. After drying with anhydrous magnesium sulfate and

Metadata

Item Type: Student Project
Creators:
CreatorsID Num. / Email
Abdul Manap, JulieyanaUNSPECIFIED
Subjects: UNSPECIFIED
Q Science > QD Chemistry > Organic chemistry > Polymers. Macromolecules
Divisions: Universiti Teknologi MARA, Shah Alam > Faculty of Applied Sciences
Item ID: 753
Uncontrolled Keywords: Synthesis, decarboxylation, dioxophenylpyrrolidine, carboxylic acid etyhl ester, magnesium sulfate
URI: http://ir.uitm.edu.my/id/eprint/753

Download

Full text not available from this repository.

Fulltext

Fulltext is available at:
UNSPECIFIED

Actions (login required)

View Item View Item