반응 #2171032

ord-02c9a548c59241ffbabe9bfffc2a24ba

반응 방정식

Cc1ccc2nc(-c3ccccc3)c(-c3ccccc3)nc2c1
6-Methyl-2,3-diphenylquinoxaline
O=C1CCC(=O)N1Br
NBS
CC(C)(C#N)N=NC(C)(C)C#N
AIBN
BrCc1ccc2nc(-c3ccccc3)c(-c3ccccc3)nc2c1
6-bromomethyl-2,3-diphenylquinoxaline

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타in dry
  2. 2
    온도to reflux
  3. 3
    workup.ADDITIONadded as a solid over a period of 30 minutes
  4. 4
    온도The solution was then refluxed for 2 hrs
  5. 5
    온도cooled
  6. 6
    세척washed with water (3×100 ml)
  7. 7
    건조dried over MgSO4
  8. 8
    기타evaporated
  9. 9
    기타to leave a pale brown solid
  10. 10
    기타This was recrystallised from hexane/toluene (1:1, 80 ml)

실험 절차

6-Methyl-2,3-diphenylquinoxaline (5.0 g, 16.9 mmol) was dissolved in dry, oxygen free benzene (50 ml). The solution was brought to reflux and a mixture of NBS (3.00 g, 16.9 mmol) and AIBN (0.1 g) added as a solid over a period of 30 minutes. The solution was then refluxed for 2 hrs, cooled, washed with water (3×100 ml), dried over MgSO4 and evaporated to leave a pale brown solid. This was recrystallised from hexane/toluene (1:1, 80 ml) to yield 6-bromomethyl-2,3-diphenylquinoxaline, 3.5 g, 56%. Traces of 6-methyl-2,3-diphenylquinoxaline were shown to be present by 1H NMR. A small sample was recrystallised from acetone for characterisation (m.pt. 146-148° C.). Found: C,; H,; N, %; C21H15N2Br requires C, 67.21; H, 4.03; N, 7.47%. 1H NMR (CDCl3, 300 MHz) δ 8.16 (d, J 8.7 Hz, 1H, Hs of quinoxaline), 8.16 (d, J 2.2 Hz, 1H, Hs of quinoxaline), 7.78 (d of d, J 8.7 Hz, J 2.2 Hz, 1H, Hs of quinoxaline), 7.48-7.56 (m, 4H, phenyl ring), 7.30-7.40 (m, 6H, phenyl ring), 4.71 (s, 2H, CH2Br).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06716371B1uspto-grants-2004_04