反応 #927237

ord-93449926e59843698ca9d007784759f4

反応方程式

[H-].[Na+]
sodium hydride
NC(=O)C(F)(F)F
trifluoroacetamide
C#CCCCCCCI
8-iodo-1-octyne
[Cl-].[NH4+]
ammonium chloride
C#CCCCCCCNC(=O)C(F)(F)F
8-trifluoroacetamido-1-octyne
収率 79.5%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added portionwise with ice cooling
  2. 2
    乾燥The ether layer was dried over magnesium sulfate
  3. 3
    濃縮concentrated under reduced pressure
  4. 4
    その他the resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent)
  5. 5
    その他crystallized from hexane

実験手順

To a solution of sodium hydride (60% oil, 9.82 g, 245 mmol) in DMF (200 ml), trifluoroacetamide (34.7 g, 307 mmol) divided into 10 portion was added portionwise with ice cooling. Then, the reaction mixture was added with a solution of 8-iodo-1-octyne (14.5 g, 61.4 mmol) in DMF (60 ml), and stirred at room temperature for two hours. The reaction mixture was added with saturated aqueous ammonium chloride (400 ml) and ether (400 ml) for extraction. The ether layer was dried over magnesium sulfate, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent), and crystallized from hexane to afford 10.8 g of 8-trifluoroacetamido-1-octyne (yield; 79.3%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06365350B1uspto-grants-2002_04