Synthesis of [1‐11C]ethyl iodide from [11C]carbon monoxide and its application in alkylation reactions
Jonas Eriksson, Gunnar Antoni, Bengt Långström
Abstract
Jonas Eriksson, Gunnar Antoni, Bengt Långström
Abstract
Abstract A method is presented for preparing [1‐11C]ethyl iodide from [11C]carbon monoxide. The method utilizes methyl iodide and [11C]carbon monoxide in a palladium‐mediated carbonylation reaction to form a mixture of [1‐11C]acetic acid and [1‐11C]methyl acetate. The acetates are reduced to [1‐11C]ethanol and subsequently converted to [1‐11C]ethyl iodide. The synthesis time was 20 min and the decay‐corrected radiochemical yield of [1‐11C]ethyl iodide was 55 ± 5%. The position of the label was confirmed by 13C‐labelling and 13C‐NMR analysis. [1‐11C]Ethyl iodide was used in two model reactions, an O‐alkylation and an N‐alkylation. Starting with approximately 2.5 GBq of [11C]carbon monoxide, the isolated decay‐corrected radiochemical yields for the ester and the amine derivatives were 45 ± 0.5% and 25 ± 2%, respectively, based on [11C]carbon monoxide. Starting with 10 GBq of [11C]carbon monoxide, 0.55 GBq of the labelled ester was isolated within 40 min with a specific radioactivity of 36 GBq/µmol. Copyright © 2004 John Wiley & Sons, Ltd.
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Abstract A method is presented for preparing [1‐11C]ethyl iodide from [11C]carbon monoxide. The method utilizes methyl iodide and [11C]carbon monoxide in a palladium‐mediated carbonylation reaction to form a mixture of [1‐11C]acetic acid and [1‐11C]methyl acetate. The acetates are reduced to [1‐11C]ethanol and subsequently converted to [1‐11C]ethyl iodide. The synthesis time was 20 min and the decay‐corrected radiochemical yield of [1‐11C]ethyl iodide was 55 ± 5%. The position of the label was confirmed by 13C‐labelling and 13C‐NMR analysis. [1‐11C]Ethyl iodide was used in two model reactions, an O‐alkylation and an N‐alkylation. Starting with approximately 2.5 GBq of [11C]carbon monoxide, the isolated decay‐corrected radiochemical yields for the ester and the amine derivatives were 45 ± 0.5% and 25 ± 2%, respectively, based on [11C]carbon monoxide. Starting with 10 GBq of [11C]carbon monoxide, 0.55 GBq of the labelled ester was isolated within 40 min with a specific radioactivity of 36 GBq/µmol. Copyright © 2004 John Wiley & Sons, Ltd.
Key concepts: Chemistry, Ethyl iodide, Carbon monoxide, Methyl iodide, Iodide, Carbonylation, Alkylation, Acetic acid