反応 #2254177

ord-6532a5d8b8de4570a8a2bbb76d5756a5

反応方程式

C=CC(F)(F)F
3,3,3-Trifluoropropene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OB(O)c1cc(Cl)cc(Cl)c1
3,5-dichlorophenylboronic acid
C=C(c1cc(Cl)cc(Cl)c1)C(F)(F)F
1,3-dichloro-5-(1-trifluoromethyl-vinyl)-benzene

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After 3 hours at reflux
  2. 2
    その他the reaction is quenched with ethyl acetate (50 ml) and water (50 ml)
  3. 3
    抽出The organic phase is then extracted with water and with a saturated aqueous solution of NaCl
  4. 4
    乾燥dried over Na2SO4
  5. 5
    濃縮concentrated in vacuo
  6. 6
    その他The crude product is purified on silica gel (35×45 mm)

実験手順

3,3,3-Trifluoropropene (3.2 g), potassium carbonate (4.6 g) and bis-(triphenylphosphine)-palladium chloride (0.2 g) is added to a solution of 3,5-dichlorophenylboronic acid in THF (20 ml) under nitrogen. After 3 hours at reflux, the reaction is quenched with ethyl acetate (50 ml) and water (50 ml). The organic phase is then extracted with water and with a saturated aqueous solution of NaCl, dried over Na2SO4 and concentrated in vacuo. The crude product is purified on silica gel (35×45 mm) using heptane (150 ml) as eluant to yield 1,3-dichloro-5-(1-trifluoromethyl-vinyl)-benzene (2.7 g), as a colorless oil. MS (HPLC/MS): no ionisation. Retention time: 5.10 min.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09044389B2uspto-grants-2015_06