反应 #10033

ord-38c716d7c7e943708a6e3647fcb2217f

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture is cooled at about 5° C.
  2. 2
    其他After separation of the phases
  3. 3
    萃取the aqueous layer is extracted with chlorobenzene (90 ml)
  4. 4
    洗涤the combined organic layers are washed with water (100 ml)
  5. 5
    其他evaporated under reduced pressure
  6. 6
    workup.ADDITIONThe obtained residue (116.9 g, containing, according to HPLC assay, 104.8 g of pure product, 88% molar yield)
  7. 7
    其他is used for the next step of the synthesis without any further purification

实验过程

To a solution of N-methylformanilide (100 g), butyl vinyl ether (74.12 g) in 85 ml of clorobenzene under stirring at 5° C., a solution of bis-trichloromethylcarbonate (87.84 g) in 170 ml of clorobenzene is added dropwise in 2 hours. The reaction mixture is kept under stirring at room temperature overnight. The mixture is cooled at about 5° C. and the pH is corrected to about 7 by adding sodium hydroxide 15% aqueous solution (348 ml). After separation of the phases, the aqueous layer is extracted with chlorobenzene (90 ml) and the combined organic layers are washed with water (100 ml) and evaporated under reduced pressure. The obtained residue (116.9 g, containing, according to HPLC assay, 104.8 g of pure product, 88% molar yield) is used for the next step of the synthesis without any further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07091382B2uspto-grants-2006_08