تفاعل #2005

ord-eb2559d3fc404f17a5ecee988d37d685

معادلة التفاعل

O
water
CC(C)O
2-propanol
Cc1ccc(B(O)O)cc1
4-tolylboronic acid
O=[N+]([O-])c1ccccc1Br
2-bromo-1-nitrobenzene
Cc1ccc(-c2ccccc2[N+](=O)[O-])cc1
product
المردود 77.4%
Cc1ccc(-c2ccccc2[N+](=O)[O-])cc1
4-Methyl-2'-nitro-1,1'-biphenyl
المردود 77.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe two-phase mixture was heated
  2. 2
    درجة الحرارةat reflux for three hours
  3. 3
    أخرىThe cooled reaction mixture
  4. 4
    ترشيحwas filtered through Celite
  5. 5
    غسيلthe filter cake washed with fresh benzene
  6. 6
    أخرىThe organic layer was separated
  7. 7
    غسيلwashed with water (3×)
  8. 8
    تجفيفdried over magnesium sulfate
  9. 9
    ترشيحfiltered
  10. 10
    أخرىThe filtrate was evaporated under vacuum
  11. 11
    أخرىthe residue (46.1 g) purified by preparative high pressure liquid chromatography on silica gel
  12. 12
    غسيلeluting with hexane/ethyl acetate (20:1)

الإجراء التجريبي

A vigorously stirred mixture of 34 g (0.25 mol) of 4-tolylboronic acid and 34 g (0.17 mol) of 2-bromo-1-nitrobenzene in a mixture of 170 mL of 5N sodium hydroxide, 57 mL of water, 215 mL of 2-propanol and 1080 mL of benzene was treated with 11.9 g of (tetrakis)triphenylphosphine palladium(0). The two-phase mixture was heated at reflux for three hours. The cooled reaction mixture was filtered through Celite and the filter cake washed with fresh benzene. The organic layer was separated and washed with water (3×), dried over magnesium sulfate and filtered. The filtrate was evaporated under vacuum and the residue (46.1 g) purified by preparative high pressure liquid chromatography on silica gel, eluting with hexane/ethyl acetate (20:1), to give 28.05 g of the product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726319uspto-grants-1998_03