A high yield synthesis of C-14-ring-labeled and C-14-methyl-labeled N-methyl-N-nitrosoaniline
✍ Scribed by C. J. Grandjean
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 232 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A synthetic procedure for C‐14‐labeled N‐methyl‐N‐nitrosoaniline is presented. Separate labeling of the methyl and phenyl side chains was achieved by using C‐14‐labeled methyl iodide and aniline, respectively. The overall yield of the four reactions was 62% and the final products were stable as stored and chemically and radiochemically pure.
📜 SIMILAR VOLUMES
## Abstract A method for incorporation of a ^14^C‐label in the ring geminal methyl moiety of Vitamin A is described. The procedure involves mono methylation of 2,6‐dimethylcyclohexanone with ^14^C‐methyl iodide as catalyzed by potassium hydride to afford 2‐^14^C, 2,6‐trimethylcyclohexanone. Subsequ
## Abstract Methyl sterculate, a cyclopropenoid fatty acid, has been synthesized with carbon‐14 as the methylene carbon in the cyclopropene ring.
Synthesis o f specific labelled [methyl-14Clsarin. The synthesis of label led [methyl-14Clsarin, [14Clmethylphosphonofluoridic acid 1-methylethyl ester, was accomplished by another approach as for nonlabelled sarin in a tele-conducted reaction vessel. The purity was estimated by IR, GC, and GC-MS a
## Abstract Labeled silver carbonate was prepared from barium carbonate‐^13^C or ‐^14^C and aqueous silver nitrate in 95 to 100% yield. Diethyl carbonate‐^13^C or ‐^14^C was generated in 60 to 85% overall yield by treatment of labeled silver carbonate with ethyl iodide and tetraethylammonium iodide