The synthesis of 14C-labeled menthol was accomplished by preparation of 14C-labeled (&) pulegone. Catalytic hydrogenation and chemical reduction converted (&) pulegone to the isomeric menthols possessing 1.10 mCi total activity. Gas chromatographic separation of this material gave the relative abund
Synthesis of 14C-labeled perfluorooctanoic and perfluorodecanoic acids; purification of perfluorodecanoic acid
✍ Scribed by Ieva L. Reich; Hans J. Reich; Lawrence A. Menahan; Richard E. Peterson
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- French
- Weight
- 397 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Perf1 uoro-n-octanoic acid (PFOA) and perf luoro-n-decanoic acid (PFOA), two yddely used industrial products, have been synthesized with C-labeling in the C-1 position. The carboxyl labeled materials were prepared in 48% and 53% yield by carbonation of perfluoroheptyllithium and perfluorononyllithium at -100°C. An efficient chemical method for purification of PFDA was also developed. Treatment of commercial PFDA with refluxing potassium hydroxide solution resulted in removal of the m n o and diprotio impurities to give 99% pure PFDA.
📜 SIMILAR VOLUMES
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.
The enzyme catalyzed displacement o f the methyl s u l f o n y l group from pentachlorophenyl methyl sulfone, the pchloroperoxybenzoic a c i d oxidation of methyl mercaptan and the reaction o f m e t h y l l i t h i u n with sulfur dioxide are methods described f o r the synthesis o f i s o t o p i
## Abstract The synthesis of indole‐3‐acetyl‐2‐^14^C‐N‐aspartic acid from carrier‐free indole‐3‐acetic acid‐2‐^14^C (54.5 mCi/mmole) and bis‐t‐butyl‐l‐aspartic acid was accomplished by coupling with dicyclohexylcarbodiimide followed by removal of the ester blocking groups by treatment with 2 N NaOH