Article

Electrophilic tetraalkylammonium nitrate nitration. II. Improved anhydrous aromatic and heteroaromatic mononitration with tetramethylammonium nitrate and triflic anhydride, including selected microwave examples.

Pfizer Global Research and Development, La Jolla Laboratories, 3550 General Atomics Court, San Diego, California 92121-1194, USA.
The Journal of Organic Chemistry (impact factor: 4.45). 02/2003; 68(2):267-75. DOI:10.1021/jo026202q pp.267-75
Source: PubMed

ABSTRACT A new one-pot nitration employing tetramethylammonium nitrate and trifluoromethanesulfonic anhydride in dichloromethane to provide a ready source of the nitronium triflate nitrating agent is presented. Rapid and selective nitration with a variety of aromatic and heteroaromatic substrates is achieved resulting in the synthesis of several novel organic compounds. A distinct advantage is the removal of undesired byproducts by aqueous workup. This very mild nitration permits large-scale syntheses and gives high isolated product yields that often require no further purification. This tetramethylammonium nitrate-based nitration also has been applied to microwave-assisted conditions, and the results with several compounds are outlined.

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Keywords

dichloromethane
 
distinct advantage
 
mild nitration permits large-scale syntheses
 
new one-pot nitration
 
nitronium triflate nitrating agent
 
novel organic compounds
 
product yields
 
selective nitration
 
tetramethylammonium nitrate
 
tetramethylammonium nitrate-based nitration
 
undesired byproducts
 

Scott A Shackelford