## Abstract Condensation of dimethoxdipheny Lmethane^14^C (III) with the levortatory (IIa) and dextrorotatory (IIb) isomers of 2‐(2‐piperidyl) ‐1, 2‐ethamediol hydrochloride, obtained respectively by hydrolysis from the d and 2 isomers (Ia and Ib) of the lower melting racemate of 2, 2‐diphenyl‐4‐(2
Synthesis of tritium and carbon-14 labeled 1,3-dioxolanes. II. D-2-ethyl-2-phenyl-4-(2-piperidyl)-1,3-dioxolane hydrochloride,
✍ Scribed by Richard S. P. Hsi
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 190 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of ^3^H and ^14^C labeled d‐2‐ethyl‐2‐phenyl‐4‐(2‐piperidyl)‐1, 3‐dioxolane hydrochloride (Va and Vb respectively) is described. The optically pure α(‐)‐2‐(2‐piperidyl)ethane‐1,2‐diol hydrochloride (II), obtained by hydrolyzing α (+)‐2,2‐diphenyl‐4‐(2‐piperidyl)‐1,3‐dioxolane hydrochloride^(1)^ (I), is used as the starting material to minimize the need for separation of isomers in the products.
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1 ,l -Oiphenyl-2-methyl-3-aminopropanol-1-"+C was prepared i n a five-step sequence o f reactions from "+C02 and resolved I n t o i t s d and 2 isomers i n an overall y i e l d o f 9.5% based on carbon-14. 1 ,l-Diphenyl-2-methyl-3-aminopropanol-3-~H was prepared by reduction o f an intermediate w l
## 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 produ
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