## Abstract In a first step, Δ1‐trans‐octenoic‐3‐^14^C acid was prepared by a Grignard reaction with BaCO~3~‐^14^C and 1‐bromo‐pentane, followed by reduction of the obtained hexanoic‐1‐^14^C acid to hexanal‐1‐^14^C via the n‐hexanol‐1‐^14^C. The produced hexanal‐1‐^14^C, by condensing with malonic
✦ LIBER ✦
Ethyl esters of Ω-carboxamidoaliphatic acids-14CONH2
✍ Scribed by V. Tolman; J. Cabak; J. Benes
- Book ID
- 102369389
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 163 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
Ethyl esters of 2‐cyanoacetic, 3‐cyanopropionic and 4‐cyanobutyric acids ‐ ^14^CN were prepared by reaction of the appropriate halogenated esters with potassium cyanide‐^14^C. Conversion of these cyanoesters into iminoether hydrochlorides and subsequent thermal decomposition gave ethyl esters of malonamic, succinamic and glutaramic acids ‐^14^CONH~2~.
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