## Abstract Phenyl [1‐^14^C] acetylene (0.012mCi/mmole) was synthesized in 12.5% yield from [1‐^14^C] acetic acid through [1‐^14^C] acetophenone, its semicarbazone, and 4‐phenyl‐[4‐^14^C] 1,2,3‐selenadiazole obtained by selenium dioxide oxidation. Oxidative coupling gave 1,4‐diphenyl [1,4‐^14^C~2~]
Synthesis of carbon-14 labeled 4-[4-[2-[2-[bis(4-chlorophenyl) methoxy]ethyl sulfonyl][1-14C]ethoxy]phenyl]-1,1,1-trifluoro-2-butanone
✍ Scribed by Douglas D. Dischino; Jacques Banville; Roger Remillard
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 91 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.655
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✦ Synopsis
Abstract
Carbon‐14 labeled 4‐[4‐[2‐[2‐[bis(4‐chlorophenyl)methoxyethylsulfonyl] [1‐^14^C]ethoxy]phenyl]‐1,1,1‐trifluoro‐2‐butanone was prepared in a six step radioactive synthesis from 2‐bromo[1‐^14^C]acetic acid. The overall radiochemical yield was 2.2%. The specific activity of the final product was found to be 42μCi/mg with a radiochemical purity of >98%. Copyright © 2002 John Wiley & Sons, Ltd.
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