Volume 18, Issue 38
Heterocyclic Compounds
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ChemInform Abstract: An Improved Preparation of 1,2,5-Triethyl-3-nitropyrrole. Friedel- Crafts Acylation with 2-Fluorobenzoyl Chloride.

M. R. PAVIA

M. R. PAVIA

Dep. Chem., Warner-Lambert/Parke-Davis Pharm. Res., Ann Arbor, MI 48105, USA

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First published: September 22, 1987

ChemInform Abstract

The activated trimethylpyrrole (I) is nitrated using potassium nitrate in concentrated sulfuric acid to produce the nitropyrrole (II) which undergoes Friedel-Crafts acylation with o-fluorobenzoyl chloride (III), yielding the 2-fluorophenyl 4'-nitropyrrol-3'-yl ketone (IV).

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