反応 #76340

ord-0ae043e1bfba43f78f3d7cfab4c39611

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他quenched with water
  2. 2
    抽出extracted with hexane
  3. 3
    乾燥The hexane layer was dried over MgSO4
  4. 4
    その他The crude product was purified by flash column chromatography on silica gel eluting with 1:10 ethyl acetate in hexane

実験手順

Ex-626A) Tetrabutylammonium iodide (0.4 g, 0.05 mol) was added to a well-stirred biphasic mixture of 12 mL of 50% NaOH and 20 mL of methylene chloride under a nitrogen atmosphere. A solution of 3-trifluoromethoxybenzaldehyde (4.0 g, 0.021 mol) and diethyl (2-oxopropyl)phosphonate (4.08 g, 0.021 mol) in 4.0 mL of methylene chloride was added dropwise to the stirred solution. The resulting mixture was stirred at room temperature for 15 min, then quenched with water and extracted with hexane. The hexane layer was dried over MgSO4. The crude product was purified by flash column chromatography on silica gel eluting with 1:10 ethyl acetate in hexane to give 2.6 g (54%) of the desired 4-[3-(trifluoromethoxy)phenyl]-3-buten-2-one product as a yellow oil. 1H NMR (CDCl3) δ7.43 (m, 4H), 7.20 (d, 1H), 6.65 (d, 2H), 2.29 (s, 3H). 19F NMR (CDCl3) δ−62.05 (s, 3F).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06699898B2uspto-grants-2004_03