反应 #2383812

ord-ec067f897f6544baa0cd6493c6c238b0

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwere added
  2. 2
    其他resulting in a white precipitate
  3. 3
    过滤The precipitate was filtered off
  4. 4
    其他the solvent was removed from the filtrate under reduced pressure

实验过程

A solution of the product of Example 6 (3.0 g, 0.0155 mol) in tetrahydrofuran (44 mL) under nitrogen was treated with a Borane.THF complex (1M, 18.56 mL) and this reaction was stirred for 2 hours. Methanol (2.50 mL) was added before a solution of saturated sodium bicarbonate (2.32 mL) and hydrogen peroxide (30%, 2.32 mL) were added resulting in a white precipitate. The precipitate was filtered off and the solvent was removed from the filtrate under reduced pressure to afford the title compound. 1H NMR (CDCl3, 300 MHz) d 1.2-2.5 (m, 8H), 2.59 (m, 2H), 2.95 (dd, 2H), 3.72 (m, 2H), 4.25 (m, 1H). 13C NMR (CDCl3, 75 MHz) d 23.87, 25.73, 26.23, 28.57, 31.88, 53.97, 61.90, 68.07, 159.9, 160.8.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06489323B1uspto-grants-2002_12