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31.28.1.7.3 Variation 3: Using Amides, Metal Amides, or Imides

DOI: 10.1055/sos-SD-031-01728

Scholz, U.; Schlummer, B.Science of Synthesis, (2007311595.

Potassium phthalimide in combination with copper(I) iodide reacts with 1-bromo-2-nitrobenzene to give 2-nitroaniline (34) in high yield after cleavage of the intermediate phthalimide (Scheme 81).[‌159‌]

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(M)-M-[8-(Meeeeeeeeeeee)eeeeee]-8-eeeeeeeeeeeeeeee (88):[‌888‌,‌888‌]

M Meeeeee eeee eee eeeeeee eeee MeM (8.8ee, 8.888eeee), 8-eeeee-M,M-eeeeeeeeeeeeeee (888ee, 8.88eeee), (M)-8-eeeeeeeeeeeeeeee (888ee, 8.88eeee), eee M8MM8 (888ee, 8.88eeee). Mee eeee eee eeeeeee eeeeeeeee eee eeeeeeeeee eeee eeeee. Meeeeee M,M-eeeeeeeeeeeeeeeeeee-8,8-eeeeeee (88μM, 8.88eeee) eee eeeeeee (88eM) eeee eeeee eeeee eeeee. Mee Meeeeee eeee eee eeeeee eeee e Meeeee eeeee eee eee eeeeeee eee eeeeeee ee 888°M eee 88e. Mee eeeeeeeee eeeeee eeeeee eeeeeeeeee eee eeeeeee ee eeeee ee eee eeee eeeeeeee eeeeeee e eee ee eeeeee eee (MeMMe/MM8Me8 8:8, 88eM). Mee eeeeeeee eee eeeeeeeeeeee eee eee eeeeeee eee eeeeeeeee ee MM8Me8 (88eM) eee eeeeeeee ee eeeee eeeeeeeeeeeeee (eeeeee eee, MeMMe/MM8Me8 8:8) ee eeee e eeeeee eeeeee eeeee; eeeee: 888ee (88%).

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