Reacción #2507819

ord-eb90ce9974ac4472a69af2a9bfcbb89c

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe batch is subsequently added to ice-cold sat. ammonium chloride soln
  2. 2
    Extracciónextracted with MTB ether
  3. 3
    Secadophases are dried over sodium sulfate
  4. 4
    Otroevaporated

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07955664B2uspto-grants-2011_06