تفاعل #56946
ord-117d740f4ce941b198f1a4abcf68544e
المتفاعلات
الكواشف
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المذيبات
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الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةat reflux under argon for 24 h
- 2تركيزThe suspension was concentrated under reduced pressure
- 3أخرىthe residue was sonicated with 1M HCl (aq) over 1.5 h
- 4أخرىThe resultant orange solid was isolated by filtration
- 5غسيلwashed with water
- 6أخرىdried
- 7أخرىsonicated with t-butyl methyl ether
- 8أخرىisolated by filtration
- 9أخرىdried
- 10أخرىWhere necessary, the product was further purified by recrystallisation
الإجراء التجريبي
4-Fluoro-3-nitrobenzoic acid (0.27 mol), an aniline (0.32 mol) and NMM (32.5 mL) in 2-methoxyethanol (750 mL) were stirred at reflux under argon for 24 h. The suspension was concentrated under reduced pressure and the residue was sonicated with 1M HCl (aq) over 1.5 h. The resultant orange solid was isolated by filtration, washed with water dried, then sonicated with t-butyl methyl ether, isolated by filtration and dried. Where necessary, the product was further purified by recrystallisation to yield the 4-anilino-3-nitrobenzoic acid: e.g. 4-(3-bromophenyl amino)-3-nitrobenzoic acid. (In some cases, for example with heteroaromatic anilines, NMN may be omitted from the reaction mixture).