反应 #1596945

ord-609d76306b6f4c51aa02b2d46b205656

反应方程式

CCCC1COC(c2ccc(OCc3ccccc3)c(F)c2)CC1Br
2-(4-benzyloxy-3-fluorophenyl)-4-bromo-5-propyltetrahydropyran
CCN(CC)CC
triethylamine
CCCC1CCC(c2ccc(O)c(F)c2)OC1
2-fluoro-4-(5-propyltetrahydropyran-2-yl)phenol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the organic phase is separated off
  2. 2
    萃取The aqueous phase is extracted with MTBE
  3. 3
    洗涤The combined organic phases are washed with water
  4. 4
    其他dried
  5. 5
    浓缩The solution is concentrated to dryness
  6. 6
    其他the residue is used directly for the following reaction

实验过程

123.0 g (0.30 mol) of 2-(4-benzyloxy-3-fluorophenyl)-4-bromo-5-propyltetrahydropyran are hydrogenated in toluene/water in the presence of Pd/C (5% of Pd) and 86.0 ml (0.60 mol) of triethylamine. The reaction solution is diluted with MTBE, and the organic phase is separated off. The aqueous phase is extracted with MTBE. The combined organic phases are washed with water and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is used directly for the following reaction.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08211513B2uspto-grants-2012_07