反应 #2507819

ord-eb90ce9974ac4472a69af2a9bfcbb89c

反应方程式

CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminium hydride
CCCC1COc2cc(C(C(=O)OCC)C(=O)OCC)c(F)cc2C1
diethyl 2-(6-fluoro-3-propylchroman-7-yl)malonate
Cl
hydrochloric acid
CCCC1COc2cc(C(CO)CO)c(F)cc2C1
2-(6-fluoro-3-propylchroman-7-yl)propane-1,3-diol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONThe batch is subsequently added to ice-cold sat. ammonium chloride soln
  2. 2
    萃取extracted with MTB ether
  3. 3
    干燥phases are dried over sodium sulfate
  4. 4
    其他evaporated

实验过程

8.7 g (21.1 mmol) of the diethyl 2-(6-fluoro-3-propylchroman-7-yl)malonate obtained under 1.2. are initially introduced in 60 ml of toluene, and 106 ml (106 mmol) of a 1 M solution of diisobutylaluminium hydride in toluene are added dropwise at 5° C. The batch is subsequently added to ice-cold sat. ammonium chloride soln., acidified using dil. hydrochloric acid and extracted with MTB ether. The combined org. phases are dried over sodium sulfate and evaporated. Chromatography of the crude product on silica gel with MTB ether/heptane (4:1) gives 2-(6-fluoro-3-propylchroman-7-yl)propane-1,3-diol as a colourless solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07955664B2uspto-grants-2011_06