反応 #88834

ord-f457df4c287242d89060fb6b3d20cb8d

反応方程式

COC(=O)c1ccc(Br)cc1Cl
4-bromo-2-chlorobenzoic acid methyl ester
C=[CH][Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC
tributyl(vinyl)tin
C=Cc1ccc(C(=O)O)c(Cl)c1
2-chloro-4-vinylbenzoic acid

溶媒

反応条件

温度
60°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The crude reaction mixture
  2. 2
    濃縮was then concentrated down
  3. 3
    ろ過filtered through a pad of celite
  4. 4
    濃縮concentrated down

実験手順

To a solution of 4-bromo-2-chlorobenzoic acid methyl ester (500 mg, 2 mmol) in THF (15 mL) was added tributyl(vinyl)tin (620 μl, 2.1 mmol) and PdCl2(dppf)-2-DCM (165 mg, 0.2 mmol). The solution was heated to 60° C. for 12 hours. The crude reaction mixture was then concentrated down and taken up in 20 mL EtOAc and 100 mL concentrated KF solution. The reaction stirred at room temperature for 3 hours, filtered through a pad of celite and concentrated down. The residual oil was subjected to flash chromatography (Isco Companion, 40 g SiO2 cartridge, solid loaded SiO2, neat heptanes to EtOAc gradient) to give 2-chloro-4-vinylbenzoic acid as a yellow oil. Amount obtained: 235 mg (60%). LCMS (M/Z): 197 (M+H). 1H NMR (Chloroform-d) δ: 3.93 (s, 3 H) 5.42 (d, J=10.9 Hz, 1 H) 5.86 (d, J=17.6 Hz, 1 H) 6.66 (dd, J=17.6, 10.7 Hz, 1 H) 7.28-7.35 (m, 1 H) 7.43-7.50 (m, 1 H) 7.82 (d, J=8.0 Hz, 1 H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09440994B2uspto-grants-2016_09