Réaction #1077250

ord-242508f100bf4f42bbaf2a698bff5a64

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreTHF was evaporated on a rotavap
  2. 2
    workup.ADDITIONThe residue was treated with water (100 mL)
  3. 3
    Extractionextracted with ether (2×100 mL)
  4. 4
    AutreRemoval of the solvent under reduced pressure

Mode opératoire

To a solution of 2-(3,4-methylenedioxy)phenylacetic acid (5 g, 25.75 mmol) in anhydrous THF (20 mL) at 0° C. was added BH3THF (40 mL, 1.0 M in THF). The mixture was stirred at room temperature for 1 h. To work up, THF was evaporated on a rotavap. The residue was treated with water (100 mL) Acidified and extracted with ether (2×100 mL). Removal of the solvent under reduced pressure gave 2-(3,4-methylenedioxy)phenyl-1-ethanol as an oil (4.7 g, 98% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06458805B2uspto-grants-2002_10