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N,N-Diethylaniline → 4-Chloro-5-nitro-6-ethylpyrimidine

HRID 129469
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HRID 129469 반응식
CCN(C1C=CC=CC=1)CC.O[C:13]1[C:18]([N+:19]([O-:21])=[O:20])=[C:17]([CH2:22][CH3:23])[N:16]=[CH:15][N:14]=1.C(OCC)(=O)C.P(Cl)(Cl)[Cl:31]>>[Cl:31][C:13]1[C:18]([N+:19]([O-:21])=[O:20])=[C:17]([CH2:22][CH3:23])[N:16]=[CH:15][N:14]=1
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참가 물질

5

반응물 4

HCID 7061N,N-DiethylanilineHCID 8857Ethyl AcetateHCID 24387Phosphorus trichlorideHCID 178437745HCID 178437745, 화합물

생성물 1

HCID 193717294-Chloro-5-nitro-6-ethylpyrimidine

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온도
60 °C

실험 절차

18.7 g (0.125 mol) of diethylaniline are dissolved in 18 ml of phosphorus chloride, and then 8.46 g (0.05 mol) of 4-hydroxy-5-nitro-6-ethylpyrimidine are stirred in. During the addition, the temperature rises from 22° to 47° C. A solution is formed which is heated at 60° C. for 2 hours. It is then stirred with ice-water and ethyl acetate for 30 minutes for the purpose of hydrolysis. The organic phase is separated off and combined with the extracts obtained by extraction, and the mixture is washed with NaHCO3 solution. Removal of the solvent yields 9.1 g of crude product, which is purified by column chromatography on silica gel (eluant:ethyl acetate/hexane 20:80 parts). 6.76 g (72.1% of the theoretical yield) of pure product are obtained in the form of an oil.

후처리

  1. additionDuring the addition
  2. customrises from 22° to 47° C
  3. customA solution is formed which
  4. customThe organic phase is separated off
  5. customobtained by extraction
  6. washthe mixture is washed with NaHCO3 solution
  7. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-dd2d483ddd3848d0a51cb0cc84f50dc8
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05468751

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