反应 #586113

ord-6d2b561264f547138e77122e85f497ac

反应方程式

O=C(N[C@H](CO)Cc1ccccc1)c1cc(OCc2ccccc2)ccc1O
N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide
O=C(N[C@H](CO)Cc1ccccc1)c1cc(O)ccc1O
N-{(S)-1-hydroxy-3-phenyl-2-propyl }-2,5-dihydroxybenzamide
收率 85.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他In a flask equipped with a magnetic stirring bar
  2. 2
    其他Nitrogen is bubbled through the solution and 10% Pd on charcoal
  3. 3
    workup.ADDITIONis added
  4. 4
    其他After flushing with nitrogen
  5. 5
    其他The suspension is flushed with nitrogen
  6. 6
    过滤filtered
  7. 7
    洗涤rinsed over Celite
  8. 8
    浓缩The filtrate is concentrated under vacuum

实验过程

In a flask equipped with a magnetic stirring bar and a rubber septum is dissolved the N-{(S)-1-hydroxy-3-phenyl-2-propyl}-5-benzyloxy-2-hydroxybenzamide in methanol. Nitrogen is bubbled through the solution and 10% Pd on charcoal is added. After flushing with nitrogen, the suspension is placed under hydrogen atmosphere and stirred for 2 hours. The suspension is flushed with nitrogen and filtered and rinsed over Celite. The filtrate is concentrated under vacuum. In this fashion is obtained N-{(S)-1-hydroxy-3-phenyl-2-propyl }-2,5-dihydroxybenzamide (85%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767646B2uspto-grants-2010_08