반응 #89705

ord-bae75d4a6891464a8177acd553e9ae94

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To an oven-dried 25 mL round-bottomed flask equipped with a magnetic stir bar and under a nitrogen gas atmosphere
  2. 2
    온도The reaction mixture was heated
  3. 3
    온도to reflux
  4. 4
    기타The volatiles were then removed in-vacuo
  5. 5
    기타the yellow oil was purified by Combiflash (10 to 30% ethyl acetate in hexanes)

실험 절차

To an oven-dried 25 mL round-bottomed flask equipped with a magnetic stir bar and under a nitrogen gas atmosphere was placed methyl(triphenylphosphoranylidene)acetate (199 mg, 0.597 mmol) and toluene (5 mL). To this heterogeneous solution was added a solution of 1,2-dibenzyl 3-tert-butyl(2S,3S)-5-oxopiperidine-1,2,3-tricarboxylate (93 mg, 0.199 mmol) in toluene (3 mL). The reaction mixture was heated to reflux and stirred overnight. The volatiles were then removed in-vacuo and the yellow oil was purified by Combiflash (10 to 30% ethyl acetate in hexanes) to afford 83 mg (80%) of 1,2-dibenzyl 3-tert-butyl(2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate. LCMS (ESI): 424 (M-CO2t-Bu+2H+), 468 (M-t-Bu+2H+), 524 (M+H+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09440958B2uspto-grants-2016_09