4-Isopropylaniline → HCID 13121218, 화합물

HRID 544387노트

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HRID 544387 반응식
Cl[C:2]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]=[CH:4][N:3]=1.[CH:10]([C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[CH:15][CH:14]=1)([CH3:12])[CH3:11]>>[CH:10]([C:13]1[CH:19]=[CH:18][C:16]([NH:17][C:2]2[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]=[CH:4][N:3]=2)=[CH:15][CH:14]=1)([CH3:12])[CH3:11]

참가 물질

3

실험 절차

To 3.6 g (0.025 mole) of 4-chloro-5,6-dimethylpyrimidine were added 3.4 g (0.025 mole) of p-isopropylaniline; the mixture was then heated at 100°-150° C. for about 3 minutes. The reaction mixture quickly became a solution and soon produced a precipitate, which was separated and then made alkaline by the addition of 50 ml of a dilute aqueous solution of sodium hydroxide. The mixture was then extracted with ethyl acetate and the extract was washed, in turn, with water and with a saturated aqueous solution of sodium chloride. It was then dried over anhydrous sodium sulphate and then the ethyl acetate was distilled off under reduced pressure, to give crystals, which, on recrystallisation froma 3:1 by volume mixture of benzene and hexane, gave 1.4 g (yield 23%) of the desired product in the form of very fine colourless needles melting at132°-133° C.

후처리

  1. temperaturethe mixture was then heated at 100°-150° C. for about 3 minutes
  2. customsoon produced a precipitate, which
  3. customwas separated
  4. additionby the addition of 50 ml of a dilute aqueous solution of sodium hydroxide
  5. extractionThe mixture was then extracted with ethyl acetate
  6. washthe extract was washed, in turn, with water and with a saturated aqueous solution of sodium chloride
  7. dry with materialIt was then dried over anhydrous sodium sulphate
  8. distillationthe ethyl acetate was distilled off under reduced pressure
  9. customto give crystals, which
  10. customon recrystallisation froma 3:1
  11. additionby volume mixture of benzene and hexane

출처 및 근거

ORD 기록
ord-74c327fdadc74d80b340c577c8ea9239
출처 데이터셋
uspto-grants-1984_05
특허 번호
US04450162

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