Synthesis of saturated fatty acids 11C(13C)-labeled in the ω-methyl position was written by Neu, Henrik;Kihlberg, Tor;Laangstroem, Bengt. And the article was included in Journal of Labelled Compounds & Radiopharmaceuticals in 1997.Synthetic Route of C15H29BrO2 This article mentions the following:
A method for the preparation of ω-labeled saturated fatty acids 11C(13C)H3(CH2)nCO2H (n = 1,2,3,,6,10,14) is described. A highly reactive zerovalent copper complex was prepared from lithium naphthalenide reduced lithium(2-thienyl)iodocuprate. The labeling precursors were obtained by addition of tert-Bu ω-iodocarboxylates to the organocuprate and these were reacted with [11C]methyl iodide to form 11C-labeled, protected intermediates. The tert-Bu ester protecting group was rapidly removed with trifluoroacetic acid, affording fatty acids 11C-labeled in the ω-Me position. A solid phase extraction method was developed and preceded final HPLC purification In a typical run starting with 2.75 GBq of [11C]methyl iodide, 375 MBq (66%) [16-11C]palmitic acid was obtained within 46 min from the end of radionuclide production In the experiment, the researchers used many compounds, for example, 15-Bromopentadecanoic acid (cas: 56523-59-2Synthetic Route of C15H29BrO2).
15-Bromopentadecanoic acid (cas: 56523-59-2) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Synthetic Route of C15H29BrO2
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary