تفاعل #1121740

ord-aeec9057008e49d596a500e417dd3173

معادلة التفاعل

C1COCCO1
1,4-dioxane
O=[N+]([O-])c1ccc(-c2cc3cc([N+](=O)[O-])ccc3o2)cc1
2-(p-nitrophenyl)-5-nitrobenzofurane
Cl
hydrochloric acid
Nc1ccc(-c2cc3cc(N)ccc3o2)cc1
2-(p-aminophenyl)-5-aminobenzofurane
المردود 90.0%

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe resulting mixture was refluxed
  2. 2
    ترشيحThe hot supernatant was filtered with Celite immediately
  3. 3
    أخرىa completion of the reaction by TLC (Thin-Layer Chromatography)
  4. 4
    غسيلThe residual material was adequately washed with hot 1,4-dioxane
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated by an evaporator
  7. 7
    تركيزAfter 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%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546049B2uspto-grants-2013_10