## Abstract Pentachloropyridine serves as a key intermediate in the synthesis of 4‐amino‐3,5,6‐trichloropicolinic acid (picloram) and 4‐amino‐3,6‐dichloropicolinic acid (aminopyralid). An M+3 stable isotope of pentachloropyridine (1, pentachloropyridine‐1‐^15^N‐2,6‐^13^C~2~) was prepared from K^13^
Highly efficient preparation of carbon-14 labeled, auxin herbicide 4-amino-3,5,6-trichloropicolinic acid
✍ Scribed by Norman R. Pearson; Tom S. Lardie
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 118 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A highly efficient, seven‐step route has been developed for the preparation of 2,6‐[^14^C~2~]‐4‐amino‐3,5,6‐trichloropicolinic acid ([^14^C~2~]‐1, 2,6‐[^14^C~2~]‐picloram) from 2,6‐[^14^C~2~]‐pentachloropyridine. The method involves the stepwise, highly selective and high yield introduction of amino and carboxylic acid groups to the 4‐ and 2‐positions, respectively, of pentachloropyridine affording [^14^C~2~]‐1 in an overall radiochemical yield of >70% with the use of only one formal purification step. Copyright © 2006 John Wiley & Sons, Ltd.
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