반응 #46764

ord-7adc86373fc74225b9d163f25c606520

용매

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was cooled to room temperature
  2. 2
    기타The heterogeneous mixture was transferred to a separatory funnel
  3. 3
    기타where the aqueous phase was separated
  4. 4
    추출re-extracted with CH2Cl2 (2×100 mL)
  5. 5
    세척washed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL)
  6. 6
    건조dried over MgSO4
  7. 7
    여과filtered
  8. 8
    농축concentrated under reduced pressure
  9. 9
    기타The residue was purified by flash chromatography on silica gel (20 to 50% ethyl acetate/hexane for elution)

실험 절차

4-Methoxy-2-nitroaniline (5 g, 0.018 mol) was dissolved in pyridine (50) and treated with menthoyl chloride (3.57 g, 0.018 mol). The reaction mixture was heated to 50° C. and stirred vigorously for 6 h. The reaction mixture was cooled to room temperature and poured into a mixture of CH2Cl2 (100 mL) and 1N HCl (100 mL)). The heterogeneous mixture was transferred to a separatory funnel where the aqueous phase was separated and re-extracted with CH2Cl2 (2×100 mL). The organic phases were combined and washed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (20 to 50% ethyl acetate/hexane for elution) provided the title compounds as colorless solid (4.9 g, 83%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741355B2uspto-grants-2010_06