## 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
Synthesis of 14C-labelled isotope-isomeric alkanes. I n-heptane-1-14C and -2-14C
✍ Scribed by Ioana Bally; Eugenia Gǎrd; Elieabeta Ciornei; Maria Biltz; A. T. Balaban
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- French
- Weight
- 301 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of n‐heptane‐1‐^14^C is described. starting from ^14^CH~3~I via (^14^CH~3~) ~2~Cd and caproyl chloride; for obtaining n‐heptane‐2‐^14^C, n‐pentyl bromide is converted into the Grignard reagent, carbonated with ^14^CO~2~, and the resulted coproic acid is converted into its chloride and treated with dimethyloadmium. In both cases the labelled n‐heptan‐2‐one is finally reduced to labelled n‐heptane by the Kishner‐Wolff method.
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