diplomsko delo
Abstract
V svojem diplomskem delu sem preizkušal aciliranje aktiviranih aromatov s karboksilnimi anhidridi in trifluoroocetno kislino. Trifluoroocetna kislina v reakciji nastopa kot katalizator in topilo. Reakcija je okolju prijaznejša alternativa klasičnemu aciliranju, kjer se uporablja kovinske kloride, ki jih v reakciji izgubimo, trifluoroocetno kislino pa je mogoče uporabiti ponovno. Ta način aciliranja daje solidne izkoristke na 1,3,5-trimetoksibenzenu in 2-metoksinaftalenu. Produkte, ki jih proizvedemo, je lahko očistiti, saj praktično ne dobimo stranskih produktov in drugih nečistot.
Keywords
aciliranje;Friedel-Craftsova reakcija;anhidridi;trifluoroocetna kislina;zelena kemija;diplomska dela;
Data
Language: |
Slovenian |
Year of publishing: |
2022 |
Typology: |
2.11 - Undergraduate Thesis |
Organization: |
UL FKKT - Faculty of Chemistry and Chemical Technology |
Publisher: |
[M. Podlipec] |
UDC: |
547.52(043.2) |
COBISS: |
124744707
|
Views: |
31 |
Downloads: |
7 |
Average score: |
0 (0 votes) |
Metadata: |
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Other data
Secondary language: |
English |
Secondary title: |
Transformations of organic compounds with carboxylic anhydrides |
Secondary abstract: |
In my thesis, I tested the alternative method of acylating aromatic compounds with carboxylic anhydrides and trifluoroacetic acid. Trifluoroacetic acid has a catalytic role in the reaction and it serves as a solvent. The reaction is a greener alternative to classic acylation where metal halides are used and are lost in the reaction. Contrary to metal halides, trifluoroacetic acid can be recycled and used for further reactions. This kind of acylation gives acceptable yields on 1,3,5-trimethoxybenzene and on 2-methoxynaphtalene. Synthesised products are easily purified because almost no by-products are formed in the process. |
Secondary keywords: |
acylation;anhydrides;trifluoroacetic acid;green chemistry;Aromatske spojine;Kemijske reakcije;Univerzitetna in visokošolska dela; |
Type (COBISS): |
Bachelor thesis/paper |
Study programme: |
1000373 |
Embargo end date (OpenAIRE): |
1970-01-01 |
Thesis comment: |
Univ. v Ljubljani, Fak. za kemijo in kemijsko tehnologijo, UNI Kemija |
Pages: |
X f., 35 str. |
ID: |
16354528 |