## Abstract Starting with benzene‐U‐^14^C, biphenyl‐U‐^14^C was synthesized in two steps in approximately 65% yield. Then two kinds of polychlorinated biphenyls‐U‐^14^C. The yield was more than 35% based on benzene‐U‐^14^C consumed.
Synthesis of 14C-labelled bis-azo biphenyl dyes
✍ Scribed by D. Franklin Milam; Robert K. Lynn
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 199 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Two 14C-label l e d bis-azo biphenyl dyes have been prepared from u n i f o r m l y r i n g -l a b e l l e d 14C-benzidine and 14C-3,3'dimethylbenzidine. The amines were t e t r a -a z o t i z e d w i t h sodium n i t r i t e and HCL. D i r e c t Blue 6 was then prepared from t e t r a -a z o benzidine by a l l o w i n g i t t o r e a c t w i t h two equival e n t s of H a c i d (8-amino-l-naphthol-3,6-disulfonic a c i d mono sodium s a l t ) under basic conditions. Acid Red 114 was prepared from t e t r a -a z o 3,3'-dirnethylbenzidine by sequential r e a c t i o n w i t h one e q u i v a l e n t o f G a c i d (2-naphthol-6,8-disulfonic a c i d dipotassium s a l t ) f o l l o w e d by one equivalent o f phenol. This product was then e s t e r i f i e d w i t h p-toluenesulfonyl c h l o r i d e t o g i v e a c i d Red 114.
📜 SIMILAR VOLUMES
## Abstract ^13^C NMR spectra of four types of azo coupling products from benzenediazonium chloride have been measured and interpreted, viz. hydrazo compounds with an intramolecular hydrogen bond (3‐methyl‐1‐phenylpyrazole‐4,5‐dione 4‐phenylhydrazone), azo compounds without an intramolecular hydrog
14C-Labelled satigrel, or 4-cyano-5-(4'-methoxy tring-U-14CI phenyl)-5-(4"methoxyphenyl)-4-pentenoic acid was synthesized for drug metabolism and pharmacokinetic studies using 4,4'-diniethoxy [ring-U-W ] benzophenone as the starting material. The radiochemical yield was 10.0%. The specific radioacti
The synthesis of 14C-labelled crotamiton, which is a fungicide, an insecticide as well as a scabicide is described. Starting from 2-bromonitrobenzene and Cu14CN, 2-toluidine, labelled with 14C at the methyl group was prepared by the following sequence of reactions : N O ~-C ~H L + -~~C O O H
## Abstract [^14^C]Aminoguanidine was synthesized by the reaction of hydrazine sulphate with barium [^14^C]cyanamide in a one‐step synthesis, and conveniently isolated by crystallization as the bicarbonate salt. The yield was 32%.