تفاعل #1121740
ord-aeec9057008e49d596a500e417dd3173
معادلة التفاعل
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةthe resulting mixture was refluxed
- 2ترشيحThe hot supernatant was filtered with Celite immediately
- 3أخرىa completion of the reaction by TLC (Thin-Layer Chromatography)
- 4غسيلThe residual material was adequately washed with hot 1,4-dioxane
- 5ترشيحfiltered
- 6تركيزconcentrated by an evaporator
- 7تركيزAfter concentration, recrystallization
الإجراء التجريبي
Then, 12.42 g (1.0 equivalent) of the obtained 2-(p-nitrophenyl)-5-nitrobenzofurane was added to 48.85 g (20.0 equivalents) of a 100 mesh iron powder previously activated by 0.5 ml of concentrated hydrochloric acid in 150 ml of a mixed solvent of 1,4-dioxane and water in proportions of 1:1, and the resulting mixture was refluxed by heating at about 110° C. for 2 hours and heavily stirred. The hot supernatant was filtered with Celite immediately after confirming a completion of the reaction by TLC (Thin-Layer Chromatography). The residual material was adequately washed with hot 1,4-dioxane and filtered. This operation was repeated three or four times, and then filtrates were combined and concentrated by an evaporator. After concentration, recrystallization was carried out with ethanol to obtain 7.1 g of orange-colored 2-(p-aminophenyl)-5-aminobenzofurane (amino compound A) at an yield of 90%.