تفاعل #46764

ord-7adc86373fc74225b9d163f25c606520

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled to room temperature
  2. 2
    أخرىThe heterogeneous mixture was transferred to a separatory funnel
  3. 3
    أخرىwhere the aqueous phase was separated
  4. 4
    استخلاصre-extracted with CH2Cl2 (2×100 mL)
  5. 5
    غسيلwashed with 1N HCl (8×100 mL), H2O (1×100 mL), 1N NaOH (2×100 mL), brine (100 mL)
  6. 6
    تجفيفdried over MgSO4
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated under reduced pressure
  9. 9
    أخرىThe residue was purified by flash chromatography on silica gel (20 to 50% ethyl acetate/hexane for elution)

الإجراء التجريبي

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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741355B2uspto-grants-2010_06