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Title:Calorimetric insight into coupling between functionalized primary alkyl halideand vinylic organocuprate reagent : experimental determination of reaction enthalpies in the synthesis of (R)-ethyl 3-(tert-butyldimethylsilyloxy)hex-5-enoate - a key lactonized statinside chain precursor
Authors:ID Časar, Zdenko (Author)
ID Tramšek, Marko (Author)
ID Goršek, Andreja (Author)
Files:.pdf Acta_Chimica_Slovenica_2010_Casar,_Tramsek,_Gorsek_Calorimetric_Insight_into_Coupling_between_Functionalized_Primary_Alkyl_Halide_and_Vi.pdf (206,94 KB)
MD5: DF4C4C556868E764BECDDD80CC6397C6
PID: 20.500.12556/dkum/0d209463-66b7-4dd6-829c-fb061b6edf02
 
URL http://acta-arhiv.chem-soc.si/57/57-1-066.pdf
 
Language:English
Work type:Scientific work
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Engineering
Abstract:The first calorimetric study of coupling between organocuprate, derived from Grignard reagent (vinyl magnesium chloride), and primary alkyl halide (e.g. (S)-ethyl 3-(tert-butyldimethylsilyloxy)-4-iodobutanoate) has been conducted. This transformation is paramountly important for efficient preparation of (R)-ethyl 3-(tert-butyldimethylsilyloxy)hex-5-enoate – a key lactonized statin side chain precursor. The results obtained give thorough calorimetric insight into this complex low-temperature synthesis as well as a new understanding of the suggested reductive elimination of the final intermediates in the coupling reaction. Namely, the surprising unexpected spontaneous three-step exothermal event has been observed during controlled progressive heating of the mixture of the final intermediates to the room temperature. This phenomenon confirms that coupling between functionalized primary alkyl halide and vinylic organocuprate reagent is not a simple $S_N2$ substitution reaction. The presented study provides among others the first reported values of reaction enthalpies and corresponding adiabatic temperature rises of reaction mixture for all exothermic events that occurred in the (R)-ethyl 3-(tert-butyldimethylsilyloxy)hex-5-enoate synthesis. The obtained results ensure consequential thermal process safety knowledge which can be incorporated into safe process scale-up as well as design of reactor system with sufficient cooling capacity for industrial production of (R)-ethyl 3-(tert-butyldimethylsilyloxy)hex-5-enoate. Moreover, the results provide a basic guidance for other organocuprate coupling reaction systems.
Keywords:Grignard reagents, organocuprates, coupling reaction, reaction calorimetry, statins
Publication status:Published
Publication version:Version of Record
Year of publishing:2010
Number of pages:str. 66-76
Numbering:Letn. 57, št. 1
PID:20.500.12556/DKUM-67419 New window
ISSN:1318-0207
UDC:547
ISSN on article:1318-0207
COBISS.SI-ID:1428828 New window
NUK URN:URN:SI:UM:DK:5GERP0DC
Publication date in DKUM:17.08.2017
Views:1254
Downloads:116
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:Acta Chimica Slovenica
Shortened title:Acta Chim. Slov.
Publisher:Slovensko kemijsko društvo
ISSN:1318-0207
COBISS.SI-ID:14086149 New window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:17.08.2017

Secondary language

Language:Slovenian
Abstract:Predstavljena je prva kalorimetrična študija reakcije med organobakrovim prekurzorjem, pripravljenim iz vinilmagnezijevega klorida, in primarnim alkilhalidom ((S)-etil 3-(terc-butildimetilsilil)-4-iodobutanoatom). Reakcija omogoča učinkovito pripravo (R)-etil 3-(terc-butildimetilsilil)heks-5-enoata, ki je ključni gradnik laktonzirane statinske stranske verige. Rezultati pridobljeni s kalorimetrično študijo omogočajo poglobljeno razumevanje te kompleksne nizko-temperaturne sinteze kot tudi novo razumevanje predpostavljene reduktivne eliminacije končnega intermediata v reakcijskem zaporedju. Opažen je bil presenetljiv nepričakovan spontan tri-stopenjski eksotermni pojav med kontroliranim postopnim segrevanjem zmesi končnega intermediata v reakcijskem mediju na sobno temperaturo. Ta pojav potrjuje dejstvo, da reakcija med primarnimi alkilhalidi in vinilnimi organobakrovimi reagenti ni enostavna $S_N2$ substitucija. Opravljena študija podaja, med drugim, tudi vrednosti reakcijskih entalpij in odgovarjajočih adiabatnih temperaturnih dvigov reakcijske zmesi za vse eksotermne pojave, ki so se zgodili med sintezo (R)-etil 3-(terc-butildimetilsilil)heks-5-enoata. Pridobljeni rezultati nam omogočajo razširitev znanja o procesih z intenzivnim sproščanjem toplote, ki ga lahko uspešno uporabimo pri varnem načrtovanju povečav tehnoloških procesov v organski sintezi in projektiranju reaktorskih sistemov z zadostno hladilno kapaciteto pri industrijski proizvodnji (R)-etil 3-(terc-butildimetilsilil)heks-5-enoata. Nadalje, rezultati študije lahko dajo osnovne smernice za podobne reakcije med organobakrovimi prekurzorji pripravljenimi iz Grignardovih reagentov in alkilhalidi.
Keywords:Grignardov reagent, reakcija spajanja, reakcijska kalorimetrija, statini


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