From: Jacob Zabicky (Jacob.Zabicky$##$uab.es)
Date: Fri Jan 01 1904 - 04:52:51 EST
Hello Abd-el-Hafeez,
At first sight it seems that besides the first one on your list, you'll
have a hard job starting from o-amino phenol. Unless it is a special
assignment you have, perhaps it will be better for the others to try
1-chloro-2-nitrobenzene or 1-bromo-2-nitrobenzene via nucleophilic
substitution with an alkoxide, followed by reduction of the nitro group.
All the best,
Jacob
>Dear all,
>I want to help me in finding a procedure for synthesis
>of five organic compounds from O-aminophenol.
>(i) O-hydroxy acetanilide.
>(ii) O-ethoxy anilide.
>(iii) O-isopropoxy aniline.
>(iv) O-cyclohexoxy aniline.
>(v) O-sec-butoxy aniline.
> thanks,
>A/Hafeez Mohamed.
>
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Group de Fisica dels Materials II Fax.: +34 93 581 2155
Universitat Autonoma de Barcelona Private Tel.: +34 93 581 7485
08193 Bellaterra (Barcelona)
Spain
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