반응 #4554

ord-0f78ba915f35468eaf7efcfa90a652a9

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The mixture was extracted with ether (2×200 ml)
  2. 2
    workup.ADDITIONPentane (100 ml) was added to the combined ether extracts
  3. 3
    세척the resulting solution washed with water (300 ml)
  4. 4
    건조The organic phase was dried (MgSO4)
  5. 5
    기타the solvent evaporated

실험 절차

A mixture of the 4-(4-bromo-2-fluorophenoxy)phenol (2.83 g, 0.01 mol), the methanesulfonate of S methyl lactate (18.2 g, 0.01 mol), and potassium carbonate (1.67 g, 0.012 mol) in DMSO (70 ml) was stirred at room temperature for 40 hours, then poured into water (700 ml). The mixture was extracted with ether (2×200 ml). Pentane (100 ml) was added to the combined ether extracts and the resulting solution washed with water (300 ml). The organic phase was dried (MgSO4) and the solvent evaporated to give a light yellow oil (~7 g). This oil was purified via prep HPLC (8:2 hexane-acetone) with the first peak being collected. Removal of the solvent gave the desired product enriched in the "R" enantiomer; Optical rotation=+20.34°@25° C. RI=1.5614@25° C.; NMR (CDCl3) was identical with that obtained in Example 4. No attempt was made to determine the optical purity of this material.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04725683uspto-grants-1988_02