反应 #325838

ord-7380437b47cf487f823e37a08c17453c

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The resulting cloudy yellow solution was re-cooled to −30° C.
  2. 2
    workup.STIRRINGThe resulting slightly yellow solution was stirred at room temperature for 3 h
  3. 3
    萃取extracted with ethyl acetate
  4. 4
    洗涤The organic layer was washed with brine
  5. 5
    干燥dried (MgSO4)
  6. 6
    过滤filtered
  7. 7
    其他purified by column chromatography on silica gel using 15-30% ethyl acetate in hexanes as eluant

实验过程

To a cold (−50° C.) suspension of methyltriphenylphosphonium bromide (1.2 g, 3.3 mmol) in tetrahydrofuran (5 mL) was added a solution of sodium bis(trimethylsilyl)-amide (3.4 mL, 3.4 mmol), and the resulting mixture was stirred for 1 h at room temperature. The resulting cloudy yellow solution was re-cooled to −30° C., and 1,1-dimethylethyl 4-(4-formyl-2-thiazolyl)-1-piperidinecarboxylate (0.5 g, 1.68 mmol) was added. The resulting slightly yellow solution was stirred at room temperature for 3 h, then diluted with water, and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), filtered, and purified by column chromatography on silica gel using 15-30% ethyl acetate in hexanes as eluant to give 471 mg of the title compound as a colorless oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08642634B2uspto-grants-2014_02