반응 #1788056

ord-b24515bd6ab3473bac446e323ce3586a

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONadded dropwise over 50 min
  2. 2
    기타the reaction mixture was evaporated under reduced pressure
  3. 3
    기타the residue was triturated with hexane
  4. 4
    기타The solid formed
  5. 5
    여과was filtered
  6. 6
    세척washed with hexane
  7. 7
    기타the combined filtrate was chromatographed on silica gel using a gradient of ethyl acetate in hexane (20%-60%) as eluent
  8. 8
    workup.DISTILLATIONDistillation under vacuum

실험 절차

A solution of methyl 3-(4-hydroxyphenyl)propionate (10.0 g, 55. 5 mmol), N-methyl-N-dodecylethanolamine (13.5 g, 55.5 mmol) and triphenylphosphine (16.0 g, 61.0 mmol) in dry tetrahydrofuran (200 ml) was treated at 22° C. with diisopropyl azodicarboxylate (12.3 g, 61.0 mmol) added dropwise over 50 min. After 3 h at 22° C., the reaction mixture was evaporated under reduced pressure and the residue was triturated with hexane. The solid formed was filtered, washed with hexane and the combined filtrate was chromatographed on silica gel using a gradient of ethyl acetate in hexane (20%-60%) as eluent. Distillation under vacuum then gave 18.0 g (75%) of 3-{4-[2-(N-dodecyl-N-methylamino)ethoxy]phenyl} propanoic acid, methyl ester as a clear oil: b.p. 180-183° C./0.02 torr (bulb to bulb distillation, air bath temperature).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06350892B1uspto-grants-2002_02