تفاعل #1462490

ord-47241199647d4ce089373cf99779e30a

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was heated at 80° C. for 24 hours
  2. 2
    استخلاصThe product was extracted with chloroform
  3. 3
    استخلاصThe chloroform extract
  4. 4
    تجفيفwas dried with anhydrous sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    workup.DISTILLATIONdistilled
  7. 7
    أخرىThe product was recrystallized from methanol
  8. 8
    أخرىa melting point of 94–95° C. (recrystallized from methanol)
  9. 9
    أخرىA 1H NMR spectrum yielded the
  10. 10
    أخرىfollowing results

الإجراء التجريبي

A 3.7 ml (0.04 mol) quantity of phosphorus oxychloride (from Aldrich) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise to the solution. The reaction mixture was heated at 80° C. for 24 hours and poured into ice water. The obtained solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde was 3.7 g (66%). The product had a melting point of 94–95° C. (recrystallized from methanol). A 1H NMR spectrum yielded the following results: (100 MHz, CDCl3, δ, ppm): 1.50 (t, J=7.0 Hz, 3H, CH3); 4.02 (q, J=7.0 Hz, 2H, CH2); 6.95–6.39 (m, 5H, Ar), 7.52–7.70 (m, 2H, Ar), 9.83 (s, 1H, CHO).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07169520B2uspto-grants-2007_01