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Sodium Hydroxide → N,N-dipropyl-2-methyl-3-nitrophenylethanamine

HRID 1436860
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HRID 1436860 반응식
C([O-])(=O)C([O-])=O.[CH3:7][C:8]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][CH:11]=[CH:10][C:9]=1[N+](CC)(CCC)CCC.[CH3:26][C:27]1C([N+]([O-])=O)=CC=C[C:28]=1[N+:36](CC)([CH2:40][CH2:41]C)[CH2:37][CH2:38][CH3:39].[OH-].[Na+]>C(OCC)(=O)C>[CH3:7][C:8]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:41][CH2:40][N:36]([CH2:37][CH2:38][CH3:39])[CH2:28][CH2:27][CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 866239722-Methyl-3-nitro-N,N-Di-n-propyl phenyl ethyl ammonium oxalate

생성물 1

HCID 13309224N,N-dipropyl-2-methyl-3-nitrophenylethanamine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

2-Methyl-3-nitro-N,N-Di-n-propyl phenyl ethyl ammonium oxalate (100 g) is added to solution of Sodium hydroxide (2000 ml 1.4%) and stir until the clear solution is obtained. Further, ethyl acetate (500 ml) is added and organic layer separated out, washed with brine solution and dried over Sodium sulphate (20 gm). Ethyl acetate is distilled out under vacuum at 50-60° C. to get residue of 2-Methyl-3-nitro-N,N-di-n-propyl phenyl ethyl amine as a free base (70-72 g)

후처리

  1. customis obtained
  2. customorganic layer separated out
  3. washwashed with brine solution
  4. dry with materialdried over Sodium sulphate (20 gm)
  5. distillationEthyl acetate is distilled out under vacuum at 50-60° C.

출처 및 근거

ORD 기록
ord-cf723a10385b462990eba506c8a07ef3
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07619095B2

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