反応 #1552105

ord-630cd77d46964731a4fa15b07690fb8f

反応方程式

Brc1ccc2nc3cc(Br)ccc3nc2c1
2,7-dibromophenazine
C=[C](OCC)[Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC
tributyl(1-ethoxyvinyl)stannane
C=C(OCC)c1ccc2nc3cc(C(=C)OCC)ccc3nc2c1
2,7-bis(1-ethoxyvinyl)phenazine
収率 88.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The crude reaction mixture
  2. 2
    ろ過was filtered through CELITE™ 545
  3. 3
    その他the volatiles were removed in vacuo
  4. 4
    その他The crude brown solid was triturated with isohexanes
  5. 5
    ろ過filtered

実験手順

To a solution of 2,7-dibromophenazine (13-2) (1.52 g, 4.50 mmol) in dry dioxane (75 mL) under N2 was added tributyl(1-ethoxyvinyl)stannane (3.34 ml, 9.89 mmol) and Pd(dppf)Cl2 (0.316 g, 0.450 mmol). The resultant mixture was heated at 100° C. for 4 hrs in a sealed tube. The crude reaction mixture was filtered through CELITE™ 545, and the volatiles were removed in vacuo. The crude brown solid was triturated with isohexanes and filtered to give 2,7-bis(1-ethoxyvinyl)phenazine as a brown solid (1.27 g, 88% yield). 1H NMR (CDCl3): δ 8.55-8.53 (2H, m), 8.19-8.15 (2H, m), 8.11-8.07 (2H, m), 4.98 (2H, d, J=3 Hz), 4.49 (2H, d, J=3 Hz), 4.03 (4H, q, J=7 Hz), 1.50 (6H, t, J=7 Hz) ppm. LC-MS (ESI): m/z 322.1 [M+H]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08999967B2uspto-grants-2015_04