تفاعل #684946

ord-75537fa6a5bc4eb78471a4412022a269

معادلة التفاعل

CCCCc1ccc(Br)cc1
1-bromo-4-butylbenzene
[Mg]
magnesium
[Na+].[OH-]
sodium hydroxide
N#Cc1nccc2ccccc12
1-isoquinolinecarbonitrile
Cl
hydrochloric acid
BrCCBr
1,2-dibromoethane
CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
title compound
CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
(4-butylphenyl)(1-isoquinolyl)ketone

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.STIRRINGwas stirred for another 1 hour at room temperature
  3. 3
    درجة الحرارةSubsequently, the solution was cooled again to 0° C.
  4. 4
    درجة الحرارةrefluxed for 2 hours
  5. 5
    ترشيحtoluene, and was filtered through celite
  6. 6
    غسيلwashed with water
  7. 7
    تجفيفdried over magnesium sulfate
  8. 8
    تركيزconcentrated
  9. 9
    أخرىThe residue was purified by silica gel column chromatography

الإجراء التجريبي

Under a nitrogen atmosphere, 1-bromo-4-butylbenzene (2.29 ml, 13.0 mmol) was added to a mixed solution of magnesium (338 mg, 13.9 mmol) and tetrahydrofuran (6.5 ml), and as an initiator, catalytic amount of 1,2-dibromoethane was added, and this was stirred under reflux for 10 minutes. The solution was cooled to 0° C., a tetrahydrofuran solution of 1-isoquinolinecarbonitrile (1.0 g, 6.49 mmol) was added, and was stirred for another 1 hour at room temperature, and at 70° C. for 3 hours. Subsequently, the solution was cooled again to 0° C., concentrated hydrochloric acid (2.56 ml) and methanol (11 ml) were added, and then refluxed for 2 hours. The concentrated residue was dissolved in 5 N sodium hydroxide and toluene, and was filtered through celite. The toluene layer of the filtrate was divided, washed with water, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography to give 1.72 g of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897387B2uspto-grants-2011_03