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1,2-Dibromoethane → methyl 1-(2-bromoethyl)-3-nitro-1H-pyrazole-5-carboxylate

HRID 1431171
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HRID 1431171 반응식
[N+:1]([C:4]1[NH:8][N:7]=[C:6]([C:9]([O:11][CH3:12])=[O:10])[CH:5]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].[Br:19][CH2:20][CH2:21]Br>CC(C)=O>[Br:19][CH2:20][CH2:21][N:7]1[C:6]([C:9]([O:11][CH3:12])=[O:10])=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[N:8]1
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참가 물질

5

반응물 3

HCID 78391,2-DibromoethaneHCID 11430Potassium CarbonateHCID 135452337methyl 3-nitro-1H-pyrazole-5-carboxylate

생성물 1

HCID 66743273methyl 1-(2-bromoethyl)-3-nitro-1H-pyrazole-5-carboxylate수율 63.4%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
0 °C

실험 절차

To a solution of methyl 5-nitro-1H-pyrazole-3-carboxylate (1 g, 5.84 mmol) in acetone (30 mL) was added potassium carbonate (4.04 g, 29.2 mmol) and 1,2-dibromoethane (3.29 g, 1.51 mL, 17.5 mmol) and the resulting solution heated to reflux for 2 h. The resulting mixture was cooled to 0° C. filtered and concentrated and the residue purified by flash chromatography (silica gel, 60 g, 20% to 40% ethyl acetate in hexanes) to give methyl 1-(2-bromoethyl)-3-nitro-1H-pyrazole-5-carboxylate (1.03 g, 63%) as a white solid.

후처리

  1. temperaturethe resulting solution heated
  2. temperatureto reflux for 2 h
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customthe residue purified by flash chromatography (silica gel, 60 g, 20% to 40% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-aa9db41a888843539742844b44b327d1
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940741B2

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