تفاعل #1470366

ord-cc921b2629564eccae075a5a5fb63624

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter this period
  2. 2
    استخلاصthen extracted into ether (3×100 ml)
  3. 3
    تجفيفThe ether extracts were dried (MgSO4)
  4. 4
    أخرىthe solvent evaporated
  5. 5
    أخرىThe residue was purified by preparative HPLC
  6. 6
    غسيلThe first peak to elute (after the solvent front)
  7. 7
    أخرىwas collected
  8. 8
    أخرىthe solvent evaporated
  9. 9
    أخرىan optical rotation of +24.68°
  10. 10
    أخرىas measured at 25° C

الإجراء التجريبي

A mixture of 4-(4-chloro-2-fluorophenoxy)phenol (2.23 g; 0.01 mole), the methanesulfonate of S methyl lactate (18.22 g; 0.1 mole, minimum of 90% optical purity), and potassium carbonate (1.4 g; 0.01 mole) in DMSO (75 ml) was stirred at room temperature for 18 hours. After this period, the mixture was poured into water (500 ml) then extracted into ether (3×100 ml). The ether extracts were dried (MgSO4), and the solvent evaporated. The residue was purified by preparative HPLC using 8:2 hexane-ethylacetate as the eluent. The first peak to elute (after the solvent front) was collected and the solvent evaporated. This gave 2.3 g (17%) of a light yellow oil whose 1H and 19F NMR (CDCl3) were consistent with the assigned structure. This material possessed an optical rotation of +24.68° as measured at 25° C. The refractive index was 1.5466. Attempts to measure the optical purity using the optically active NMR shift reagent tris-[3-(trifluoromethylhydroxymethylene)-d-camphorateo]europium (III) were not successful. Based upon the optical purity of the starting lactate the optical purity is estimated to be between 75 and 95%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04808750uspto-grants-1989_02