diplomsko delo
Lana Jamnik (Author), Uroš Grošelj (Mentor)

Abstract

V diplomski nalogi sem opisala eno od možnih sinteznih poti do (R)-2-(2-bromoetil)-1,1-dimetil-5-metilenciklopentana iz komercialno lahko dostopne kafre. Opisala sem vse sintezne korake s poudarkom na Appelovi reakciji. Večji del te sinteze sem izvedla tudi v laboratoriju. Pripravila sem (R)-4-(2-bromoetil)-1,5,5-trimetilciklopent-1-en iz (1S)-(+)-10-kafrasulfonske kisline. Sintezo sem izvedla v štirih korakih preko (+)-izokamfolenske kisline, ki nastane z Grobovo fragmentacijo. Ključni korak sinteze je bila tvorba bromida iz alkohola pod blagimi reakcijskimi pogoji, ki jih zagotavlja Appelova reakcija.

Keywords

kafrasulfonska kislina;Grobova fragmentacija;Appelova reakcija;diplomska dela;

Data

Language: Slovenian
Year of publishing:
Typology: 2.11 - Undergraduate Thesis
Organization: UL FKKT - Faculty of Chemistry and Chemical Technology
Publisher: [L. Jamnik]
UDC: 547.599.6(043.2)
COBISS: 159909635 Link will open in a new window
Views: 60
Downloads: 47
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Other data

Secondary language: English
Secondary title: Synthesis of (R)-4-(2-bromoethyl)-1,5,5-trimethylcyclopent-1-ene
Secondary abstract: In my thesis, I described one of the possible synthesis routes of (R)-2-(2-bromoethyl)-1,1-dimethyl-5-methylenecyclopentane from commercially readily available camphor. I described all the synthesis steps, with an emphasis on the Appel reaction. I also carried out the major part of this synthesis in the laboratory. I prepared (R)-4-(2-bromoethyl)-1,5,5-trimethylcyclopent-1-ene from (1S)-(+)-10-camphorsulfonic acid. I carried out the synthesis in four steps via (+)-isocampholenic acid, which is formed by Grob fragmentation. The key step of the synthesis was the formation of the bromide from the alcohol under mild reaction conditions provided by the Appel reaction.
Secondary keywords: camphor;camphorsulfonic acid;Grob fragmentation;Appel reaction;Organska sinteza (kemija);Kafra;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: 44 str.
ID: 19356513