反应 #6685

ord-1f6cb91870914577b79f39714d7ce277

反应方程式

Fc1cccc(OCCCCOC2CCCCO2)c1F
2-[4-(2,3-difluorophenoxy)-butoxy]-tetrahydropyran
Fc1cccc(OCCCCOC2CCCCO2)c1F
2-[4-(2,3-Difluorophenoxy)butoxy]-tetrahydropyran
Cc1ccc(S(=O)(=O)O)cc1
para-toluenesulfonic acid
OCCCCOc1cccc(F)c1F
4-(2,3-difluorophenoxy)-butan 1-ol
OCCCCOc1cccc(F)c1F
4-(2,3-Difluorophenoxy)-butan-1-ol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他quenched with water
  2. 2
    萃取extracted with ethyl acetate:hexane (1:1)
  3. 3
    洗涤washed with brine
  4. 4
    干燥dried over MgSO4
  5. 5
    浓缩concentrated in vacuo
  6. 6
    其他Purification by chromatography on silica gel (10% EtOAc/hexanes)

实验过程

To a solution of 2-[4-(2,3-difluorophenoxy)-butoxy]-tetrahydropyran (20) (1 equi.) and commercially available para-toluenesulfonic acid (21) (0.1 equi.) in methanol:THF (1:1) (3 mL/mmole), water (0.005 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane (1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (10% EtOAc/hexanes) gave 4-(2,3-difluorophenoxy)-butan 1-ol (22), as a white solid (84%)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07083832B2uspto-grants-2006_08