z-logo
Premium
The synthesis of 14 C‐labelled (U) 2,4,2′,4′‐tetrachlorobiphenyl
Author(s) -
Melvas B.
Publication year - 1974
Publication title -
journal of labelled compounds
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0022-2135
DOI - 10.1002/jlcr.2590100217
Subject(s) - thionyl chloride , yield (engineering) , chlorine , ampoule , chemistry , benzene , condensation , nuclear chemistry , nitro , organic chemistry , chloride , radiochemistry , medicinal chemistry , materials science , metallurgy , physics , alkyl , thermodynamics
It was possible to prepare 14 C‐2,4,2′,4′‐tetrachlorobiphenyl with a purity of 98% by condensation of 14 C‐1‐chloro‐2,4‐dinitro‐benzene to yield 14 C‐2,4,2′,4′,‐tetranitrobiphenyl and substitution of the nitro groups by chlorine with thionyl chloride. The synthesis must be carried out on a small scale for two reasons‐the cost and the hazards with radioactive material. The synthesis described here was performed on a 10mg scale. Both of the chemical reactions were performed in sealed ampoules and the overall yield varied between 30 and 40%.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom