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1,1-Dimethylhydrazine → N'-(5-chloroindan-1-ylidene)-N,N-dimethylhydrazine

HRID 1977820
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HRID 1977820 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=O)[CH2:6][CH2:5]2.[CH3:12][N:13]([CH3:15])[NH2:14].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[N:14][N:13]([CH3:15])[CH3:12])[CH2:6][CH2:5]2
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참가 물질

5

반응물 3

HCID 59761,1-DimethylhydrazineHCID 6101p-Toluenesulfonic acidHCID 1425995-Chloro-1-indanone

생성물 1

HCID 57200018N'-(5-chloroindan-1-ylidene)-N,N-dimethylhydrazine

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

20 g of 5-chloroindan-1-one are dissolved in 600 ml of dry toluene and, after addition of 27.4 ml of N,N-dimethylhydrazine and 1 g of p-toluenesulfonic acid, boiled with a water trap for 4 h. The reaction mixture is concentrated in vacuo, and the residue is dissolved in ethyl acetate and washed with sodium bicarbonate solution and then with water. The organic phase is dried over sodium sulfate and concentrated in vacuo, and the residue is chromatographed on silica gel with ethyl acetate/heptane ½. N′-(5-chloroindan-1-ylidene)-N,N-dimethylhydrazine is obtained as an oil.

후처리

  1. concentrationThe reaction mixture is concentrated in vacuo
  2. dissolutionthe residue is dissolved in ethyl acetate
  3. washwashed with sodium bicarbonate solution
  4. dry with materialThe organic phase is dried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customthe residue is chromatographed on silica gel with ethyl acetate/heptane ½

출처 및 근거

ORD 기록
ord-108fb2fe712e458dba64e7e62fd662e1
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06235763B1

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