تفاعل #2069942

ord-77bacd3e7e8a4bc5af5c9678b264cc01

معادلة التفاعل

Cl
hydrochloric acid
CCCCc1ccc(Br)cc1
1-Bromo-4-butylbenzene
BrCCBr
1,2-dibromoethane
[Mg]
magnesium
C1CCOC1
tetrahydrofuran
N#Cc1nccc2ccccc12
1-isoquinolinecarbonitrile
C1CCOC1
tetrahydrofuran
CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
title compound
CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
(4-Butylphenyl)(1-isoquinolyl)ketone

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder reflux for 10 minutes
  2. 2
    workup.STIRRINGthis mixture was stirred at room temperature for 1 hour
  3. 3
    درجة الحرارةThereafter, the mixture was cooled again to 0° C.
  4. 4
    درجة الحرارةthis mixture was heated
  5. 5
    درجة الحرارةunder reflux for 2 hours
  6. 6
    تركيزAfter the mixture was concentrated
  7. 7
    workup.DISSOLUTIONthe residue was dissolved in 5 N sodium hydroxide
  8. 8
    ترشيحtoluene, and was filtered through celite
  9. 9
    أخرىThe toluene layer of the filtrate was separated
  10. 10
    غسيلwashed with water
  11. 11
    تجفيفdried over anhydrous magnesium sulfate
  12. 12
    تركيزconcentrated under reduced pressure
  13. 13
    أخرىThe residue was purified by silica gel column chromatography

الإجراء التجريبي

1-Bromo-4-butylbenzene (2.29 ml, 13 mmol) and a catalytic amount of 1,2-dibromoethane as an initiator were added to a mixed solution of magnesium (338 mg, 14 mmol) and tetrahydrofuran (6.5 ml) under nitrogen atmosphere, and this mixture was stirred under reflux for 10 minutes. The mixture was cooled to 0° C., a solution of 1-isoquinolinecarbonitrile (1.0 g, 6.5 mmol) in tetrahydrofuran was added, and this mixture was stirred at room temperature for 1 hour, then at 70° C. for 3 hours. Thereafter, the mixture was cooled again to 0° C., concentrated hydrochloric acid (2.6 ml) and methanol (11 ml) were added, and this mixture was heated under reflux for 2 hours. After the mixture was concentrated, the residue was dissolved in 5 N sodium hydroxide and toluene, and was filtered through celite. The toluene layer of the filtrate was separated, washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (1.7 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07541332B2uspto-grants-2009_06