## Abstract Synthesis of n‐heptane labelled with carbon‐14 in the 1‐position is described. The precedure involves five steps starting with reaction of [^14^C]carbon dioxide with n‐hexyl magnesium bromide and finishing with reduction of [1‐^14^C]n‐heptyl bromide. The purity of the final product was
The new “one-flask” synthesis of 14C labelled 1-bromoalkanes - synthesis of 1-bromo [1-14c] heptane
✍ Scribed by Tomáš Elbert; Jiří Filip
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 407 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Conditions were found for almost quantitative carboxylation of n-hexyllithium with l4CO2 to afford lithium [1-l4C] heptanoate.
It was then possible to perform the reaction sequence lithium [1-l4C] heptanoate --+ [l-14C] heptan-1-01 + 1-bromo [l-14q heptane in one flask without isolation of intermediates. In the "hot" synthesis 12,8 GBq (346 mCi) of 1-bromo [l-14CJ heptane with radiochemical purity better than 97 % were prepared from Bal4CO3 in 81 % yield.
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