反应 #1269905

ord-e45a071ae9e449a0960e3984b1a85b50

反应方程式

Fc1ccc2c(c1)C1(CCN(Cc3ccccc3)CC1)OC2
1′-benzyl-6-fluoro-3H-spiro[2-benzofuran-1,4′-piperidine]
Fc1ccc2c(c1)C1(CCNCC1)OC2
6-fluoro-3H-spiro[2-benzofuran-1,4′-piperidine]
收率 96.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture was refluxed under an hydrogen atmosphere for 8 hours
  2. 2
    其他purged with argon
  3. 3
    过滤The catalyst was filtered
  4. 4
    浓缩the filtrate was concentrated in vacuo

实验过程

To a solution of 1′-benzyl-6-fluoro-3H-spiro[2-benzofuran-1,4′-piperidine] (1 g, 3.4 mmol) in ethanol (10 ml) was added Pd/C 10% (100 mg, 0.09 mmol). The mixture was refluxed under an hydrogen atmosphere for 8 hours then cooled to room temperature and purged with argon. The catalyst was filtered and the filtrate was concentrated in vacuo to yield 0.67 g (96%) 6-fluoro-3H-spiro[2-benzofuran-1,4′-piperidine] as a white solid. MS m/e: 208 (M+H+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08664216B2uspto-grants-2014_03