反応 #46764

ord-7adc86373fc74225b9d163f25c606520

溶媒

反応条件

温度
50°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was cooled to room temperature
  2. 2
    その他The heterogeneous mixture was transferred to a separatory funnel
  3. 3
    その他where the aqueous phase was separated
  4. 4
    抽出re-extracted with CH2Cl2 (2×100 mL)
  5. 5
    洗浄washed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL)
  6. 6
    乾燥dried over MgSO4
  7. 7
    ろ過filtered
  8. 8
    濃縮concentrated under reduced pressure
  9. 9
    その他The residue was purified by flash chromatography on silica gel (20 to 50% ethyl acetate/hexane for elution)

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741355B2uspto-grants-2010_06