Nitric Acid → 4-Ethyl-2-nitroaniline

HRID 326623

반응식

HRID 326623 반응식
[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1)[CH3:2].[N+:10]([O-])([OH:12])=[O:11]>C(OC(=O)C)(=O)C>[CH2:1]([C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[C:5]([N+:10]([O-:12])=[O:11])[CH:4]=1)[CH3:2]

참가 물질

4

반응 조건

온도
10 °C

실험 절차

To acetic anhydride (160 ml) at room temperature was added 4-ethylaniline (30 g) over 15 minutes with stirring. The mixture was cooled to 10° C. and concentrated nitric acid (45 ml) was added very slowly, keeping the reaction temperature to below 14° C. The mixture was warmed to room temperature over one hour, poured into ice-water and the resultant yellow solid was filtered off and dried. This was added to dioxan (100 ml), followed by 6M hydrochloric acid (100ml), the solution heated to 70° C. for 3 hr, poured into water, and 1M sodium hydroxide added until pH 10. The product was extracted into ethyl acetate which was then washed with water, brine, dried over magnesium sulphate and solvent removed under vacuum to give 4-ethyl-2-nitroaniline (28.4 g). δ (60 MHz CDCl3) 1.2 (3H, t, CH3), 2.5 (2H, q, CH2). 6.3 (2H. bs, NH2 ) and 6.6 to 7.8 (3H, m, ArH).

후처리

  1. customto below 14° C
  2. temperatureThe mixture was warmed to room temperature over one hour
  3. filtrationthe resultant yellow solid was filtered off
  4. customdried
  5. additionThis was added to dioxan (100 ml)
  6. temperaturethe solution heated to 70° C. for 3 hr
  7. additionpoured into water, and 1M sodium hydroxide
  8. additionadded until pH 10
  9. extractionThe product was extracted into ethyl acetate which
  10. washwas then washed with water, brine
  11. dry with materialdried over magnesium sulphate and solvent
  12. customremoved under vacuum

출처 및 근거

ORD 기록
ord-bad840f2a61641a192a6987d903bb2e9
출처 데이터셋
uspto-grants-1993_12
특허 번호
US05270309

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