## Abstract A versatile method for ^14^C labeling of 2‐methoxypyrimidine‐5‐carboxylic acid at the 2‐position has been developed after encountering difficulties with traditional approaches to label the carboxyl function. The method developed can also be used for ^14^C labeling other positions of the
Synthesis of 14c-labeled 2,2-dichloropropionic acid
✍ Scribed by F. S. Tanaka; R. G. Wien
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 413 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A widely used herbicide, 2,2‐dichloropropionic acid (dalapon), was synthesized with ^14^C‐labeling in the C‐1 or C‐2 positions. The carboxyl labeled material was prepared in 55% yield by carbonation of 1,1‐dichloro‐ethyllithium at approximately −104°. Starting with trichloroacetic acid, the C‐2 labeled product was prepared in an overall yield of 39% by means of a 4‐step reaction sequence which involved the removal of a chlorine atom and the addition of a methyl group.
📜 SIMILAR VOLUMES
A synthesis of dibucaine labeled with l"C in the heterocyclic ring is described. starting with isatin and acetic anh~dride-2-~"C as shown in Scheme I. Two deutero analogs, dibucaine-d2 and dibucaine-dg, were also synthesized by the reactions shown in Scheme 11. Dibucaine-dg was synthesized by conden
## Abstract A convenient procedure to synthesize 2–^14^C‐dinitroso‐hexahydropyrimidine (DNHP) is described. The synthesis begines with the condensation of ^14^C‐formaldehyde and propylenediamine‐1,3 in benzene with azeotropic removal of water. The resulting bases are isolated from the reaction mixt
14C-labeled chlorogenic acid (specijic activity 30.6 nCilmg) was synthesized by reaction of diphenylmethyl-I-0-ethoxy-carbonyl- 4,5-0-isopropylidenequinate ( V ) with 0,O-dimethylcarbonyl caffeoyl chloride-u-14C (VIII) followed by selective hydrolysis of the protecting groups.