تفاعل #66032

ord-ea826ef5f5ee438782a80e86607ef50a

معادلة التفاعل

COc1ccc(Br)c2ccccc12
1-Bromo-4-methoxynaphthalene
OB(O)c1ccc(-c2cccc3ccccc23)cc1
4-(naphthalen-1-yl)phenylboronic acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O
water
COc1ccc(-c2ccc(-c3cccc4ccccc34)cc2)c2ccccc12
product
المردود 52.6%
COc1ccc(-c2ccc(-c3cccc4ccccc34)cc2)c2ccccc12
1-methoxy-4-{4-(naphthalen-1-yl)phenyl}naphthalene
المردود 52.6%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder reflux
  2. 2
    أخرىAfter completion of the reaction
  3. 3
    استخلاصextracted with ethyl acetate (300 mL) and water (1000 mL)
  4. 4
    تجفيفThe organic layer was dried with magnesium sulfate
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىto obtain a solid
  7. 7
    ترشيحfiltered
  8. 8
    أخرىThe filtrate was recrystallized in methanol (800 mL)
  9. 9
    ترشيحThe resultant solid was filtered
  10. 10
    غسيلwashed with hexane (300 mL)

الإجراء التجريبي

1-Bromo-4-methoxynaphthalene (25 g, 0.105 mol), 4-(naphthalen-1-yl)phenylboronic acid (30.4 g, 0.137 mol), potassium carbonate (21.9 g, 0.16 mol), tetrakis(triphenylphosphine)palladium(0) (2.4 g, 0.01 mol), water (25 mL), tetrahydrofuran (75 mL) and toluene (75 mL) were stirred in a 250 mL round-bottom flask for 12 hours under reflux. After completion of the reaction, the reaction mixture was cooled to room temperature and extracted with ethyl acetate (300 mL) and water (1000 mL). The organic layer was dried with magnesium sulfate and concentrated under reduced pressure to obtain a solid. The solid was dissolved in hot toluene (400 mL) and then filtered. The filtrate was recrystallized in methanol (800 mL). The resultant solid was filtered and washed with hexane (300 mL) to obtain a product (20 g, 0.055 mol, 52.6%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524381B2uspto-grants-2013_09