反应 #50044

ord-b7584f1f3ebc4e52879c9f889abda715

溶剂

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled to 0° C.
  2. 2
    其他quenched by careful addition of 10% acetic acid in methanol
  3. 3
    其他The mixture was reduced in volume on a rotary evaporator
  4. 4
    workup.DISSOLUTIONthe concentrate was dissolved in ethyl acetate
  5. 5
    洗涤which was washed successively with 1N HCl, water and sodium bicarbonate solution
  6. 6
    萃取The organic extract
  7. 7
    干燥was dried over Na2SO4
  8. 8
    浓缩concentrated

实验过程

A 21.56 g (86.55 mmol) sample of the compound from step 24a above was dissolved in 200 mL of THF, and the solution was cooled to 0° C. BH3 -dimethyl sulfide (86.5 mL, 2N) was added dropwise under a nitrogen atmosphere. The reaction was stirred at room temperature for 16 hr, then cooled to 0° C. and quenched by careful addition of 10% acetic acid in methanol. The mixture was reduced in volume on a rotary evaporator, and the concentrate was dissolved in ethyl acetate, which was washed successively with 1N HCl, water and sodium bicarbonate solution. The organic extract was dried over Na2SO4 and concentrated to afford the title product, 19.94 g (98% yield).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05424444uspto-grants-1995_06