تفاعل #1509643

ord-3ec6cdd74f694e62ac0de91d7d5ef30e

معادلة التفاعل

OB(O)c1ccc(N(c2ccccc2)c2ccccc2)cc1
(4-(diphenylamino)phenyl)boronic acid
Brc1ccc(I)cc1
4-iodo-1-bromobenzene
O=C([O-])[O-].[Na+].[Na+]
Na2CO3
Brc1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1
Compound 35
المردود 87.0%
Brc1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1
4′-bromo-N,N-diphenyl-[1,1′-biphenyl]-4-amine
المردود 87.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas degassed
  2. 2
    درجة الحرارةthe resulting mixture was heated
  3. 3
    درجة الحرارةat reflux overnight under an argon atmosphere
  4. 4
    درجة الحرارةAfter cooling
  5. 5
    workup.ADDITIONthe mixture was poured into dichloromethane (150 mL)
  6. 6
    غسيلwashed with water (2×150 mL) and brine (100 mL)
  7. 7
    تجفيفThe organic phase was dried over Na2SO4
  8. 8
    أخرىpurified with flash column chromatography (silica gel, hexanes/ethyl acetate 50:1)
  9. 9
    أخرىthen recrystallized in dichloromethane/methanol

الإجراء التجريبي

A mixture of (4-(diphenylamino)phenyl)boronic acid (1.5 g, 5.19 mmol), 4-iodo-1-bromobenzene (1.33 g, 4.71 mmol), Na2CO3 (1.78 g, 16.8 mmol) and Pd(PPh3)4 (0.163 g, 0.141 mmol) in THF/H2O (28 mL/17 mL) was degassed and the resulting mixture was heated at reflux overnight under an argon atmosphere. After cooling, the mixture was poured into dichloromethane (150 mL), then washed with water (2×150 mL) and brine (100 mL). The organic phase was dried over Na2SO4, purified with flash column chromatography (silica gel, hexanes/ethyl acetate 50:1) then recrystallized in dichloromethane/methanol to afford a white solid (Compound 35)(1.64 g, in 87% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927121B2uspto-grants-2015_01