반응 #9049

ord-08381d0f80044bf994b13f6803c6eb40

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The resultant brown precipitate was filtered
  2. 2
    세척washed with CH2Cl2
  3. 3
    workup.ADDITIONThe filtrate was diluted with EtOAc (40 mL) and water (30 mL)
  4. 4
    세척the organic phase washed with brine (1×30 mL)
  5. 5
    건조dried (Na2SO4)
  6. 6
    농축concentrated under reduced pressure
  7. 7
    기타The resultant yellow oil was purified by column chromatography on silica gel (4:1 Hexanes/EtOAc)

실험 절차

To a stirred solution of N-hydroxyphthalimide (0.60 g, 3.68 mmol) and Et3N (0.60 mL, 4.30 mmol) in DMF (6 mL) was added α,α′-dibromo-o-xylene (3.30 g, 0.0125 mol) and the mixture stirred at room temperature for 4 h. The resultant brown precipitate was filtered and washed with CH2Cl2. The filtrate was diluted with EtOAc (40 mL) and water (30 mL) and the organic phase washed with brine (1×30 mL), dried (Na2SO4) and concentrated under reduced pressure. The resultant yellow oil was purified by column chromatography on silica gel (4:1 Hexanes/EtOAc) to give the title compound (581 mg, 46%) as a white solid. 1H NMR (CDCl3) δ 4.99 (s, 2H), 5.37 (s, 2H), 7.27–7.40 (m, 2H), 7.41–7.45 (m, 2H), 7.73–7.76 (m, 2H), 7.81–7.84 (m, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091217B2uspto-grants-2006_08