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Synthesis of ring-14C-labelled 4(3′-, 6′-dimethyl-3′-heptyl)-phenol

✍ Scribed by J. O. Lalah; D. Lenoir; B. Henkelmann; N. Hertkorn; K. Günther; K.-W. Schramm; A. Kettrup


Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
79 KB
Volume
44
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

Ring‐^14^C‐labelled 4(3′‐, 6′‐, dimethyl‐3′‐,heptyl)‐phenol (NP), an isomer of paranonyl phenol was synthesized for use in aquatic toxicity and metabolism studies. A very efficient method involving alkylation of ring‐^14^C‐labelled anisole and tertiary alkyl bromide (3‐bromo‐3,6‐dimethyl heptane) with AlCl~3~ followed by cleavage of the resultant ether with BBr~3~ was used giving a 24% yield ring labelled ^14^C‐NP (specific activity: 16.205 MBq/mg and purity >95% by HPLC) after TLC separation. Copyright © 2001 John Wiley & Sons, Ltd.


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