تفاعل #95100

ord-99133378138d4a53a7c17c71f1a63b52

معادلة التفاعل

CC(Br)C(=O)c1ccccc1
2-bromo-propiophenone
Nc1ccc(OCc2ccccc2)cc1
4-benzyloxy-aniline
Cc1c(-c2ccccc2)[nH]c2ccc(OCc3ccccc3)cc12
5Benzyloxy-3-methyl-2-phenyl-1H-indole

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was evaporated to dryness
  2. 2
    درجة الحرارةthe residue was heated for two hours to 180° C
  3. 3
    درجة الحرارةAfter cooling
  4. 4
    workup.ADDITIONthe residue was mixed with 10% hydrochloric acid
  5. 5
    استخلاصextracted with chloroform
  6. 6
    تجفيفThe extracts were dried over sodium sulfate
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated
  9. 9
    أخرىThe residue obtained
  10. 10
    أخرىwas purified by column chromatography on silicagel with toluene as solvent

الإجراء التجريبي

An amount of 3.6 g (0.015 mole) of 2-bromo-propiophenone and 6 g (0.03 mole) of 4-benzyloxy-aniline were refluxed for two hours in 15 ml of triethylamine. The mixture was evaporated to dryness, and the residue was heated for two hours to 180° C. After cooling, the residue was mixed with 10% hydrochloric acid and extracted with chloroform. The extracts were dried over sodium sulfate, filtered, and evaporated. The residue obtained was purified by column chromatography on silicagel with toluene as solvent.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04343811uspto-grants-1982_08