反応 #6691

ord-96173bef1136419e80caf61235bb990a

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他quenched with water
  2. 2
    抽出extracted with ethyl acetate:hexane (1:1)
  3. 3
    洗浄washed with brine
  4. 4
    乾燥dried over MgSO4
  5. 5
    濃縮concentrated in vacuo
  6. 6
    その他Purification by chromatography on silica gel (10% EtOAc/hexanes)

実験手順

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%).

出典

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