Réaction #1772065

ord-61b58ad0d6a14a958a46001cc7b86406

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreevaporated to dryness under reduced pressure
  2. 2
    workup.ADDITIONEtOAc (100 mL) and saturated aqueous NaHCO3 (100 mL) were added
  3. 3
    Extractionthe aqueous phase was extracted with EtOAc (3×100 mL)
  4. 4
    SéchageThe organic fractions were dried with MgSO4
  5. 5
    Autreevaporated under reduced pressure

Mode opératoire

(R)-Mandelic acid (2.568 g, 16.87 mmol) and 2,2-dimethoxypropane (5.1 mL, 41.48 mmol) were dissolved in MeOH (100 mL) and 12M HCl (100 mL) was added. The resulting solution was stirred for 20 hr under a CaCl2 tube and evaporated to dryness under reduced pressure. EtOAc (100 mL) and saturated aqueous NaHCO3 (100 mL) were added, and the aqueous phase was extracted with EtOAc (3×100 mL). The organic fractions were dried with MgSO4, and evaporated under reduced pressure to give (R)-methyl mandelate, (R)-4, quantitatively (2.78 g) as a white solid which was of sufficient purity for the next step.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08148128B2uspto-grants-2012_04