反応 #80193

ord-36cbd75478f8477dab52b6816e964839

反応方程式

CCOC(=O)c1cccnc1Cl
Ethyl 2-chloro-nicotinate
OB(O)c1ccc(C(F)(F)F)cc1
4-trifluoromethylphenylboronic acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCOC(=O)c1cccnc1-c1ccc(C(F)(F)F)cc1
brown oil
収率 109.7%
CCOC(=O)c1cccnc1-c1ccc(C(F)(F)F)cc1
2-(4-Trifluoromethyl-phenyl)-nicotinic acid ethyl ester
収率 109.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the reaction vessel purged
  2. 2
    温度The reaction mixture was heated at 90 C
  3. 3
    温度for 1.5 h before being cooled
  4. 4
    抽出extracted with 150 ml of ether
  5. 5
    洗浄The organic layer was washed with 50 ml of 2N NaOH, 2×50 ml water, and brine
  6. 6
    乾燥before being dried (magnesium sulfate)
  7. 7
    ろ過filtered
  8. 8
    濃縮concentrated under vacuum

実験手順

Ethyl 2-chloro-nicotinate (1.86 g, 10.0 mmol) was dissolved in 10 ml of dimethoxyethane. Tetrakis(triphenylphosphine)palladium (347 mg, 0.3 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. A solution of 4-trifluoromethylphenylboronic acid (2.09 g, 11.0 mmol) in 20 ml of dimethoxyethane was added to the reaction mixture followed by 10 ml of a 2M sodium carbonate solution. The reaction mixture was heated at 90 C. for 1.5 h before being cooled and extracted with 150 ml of ether. The organic layer was washed with 50 ml of 2N NaOH, 2×50 ml water, and brine before being dried (magnesium sulfate), filtered and concentrated under vacuum to afford 3.24 g of a brown oil. This material was purified by silica gel chromatography eluting with 5 to 10% ethyl acetate in hexanes to afford 2.34 g of the title compound as a pale yellow oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06713489B2uspto-grants-2004_03