Potassium Carbonate → Ethyl 3-[1-(4-methyl-2-nitrophenyl)-1H-imidazol-2-yl]-propanoate

HRID 72771ノート

反応式

HRID 72771 の反応式
F[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[NH:12]1[CH:16]=[CH:15][N:14]=[C:13]1[CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20].C(=O)([O-])[O-].[K+].[K+].CN(C)C(=O)C>C(OCC)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([N:12]2[CH:16]=[CH:15][N:14]=[C:13]2[CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[C:3]([N+:9]([O-:11])=[O:10])[CH:4]=1

参加物

6

反応物 4

HCID 11430Potassium CarbonateHCID 31374DimethylacetamideHCID 1362874-Fluoro-3-nitrotolueneHCID 22259341Ethyl 3-(1H-imidazol-2-YL)propanoate

生成物 1

HCID 59198588Ethyl 3-[1-(4-methyl-2-nitrophenyl)-1H-imidazol-2-yl]-propanoate収率 92.9%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

1-Fluoro-4-methyl-2-nitrobenzene 239 mg, ethyl 3-(1H-imidazol-2-yl)propanoate 252 mg, potassium carbonate 415 mg and N,N-dimethylacetamide 10 mL were stirred at 100° C. for 11.5 hours, and then at 130° C., for 6 hours. The reaction liquid was diluted with diethyl ether, washed with water and saturated brine by the order stated, and dried over magnesium sulfate. Distilling the solvent off under reduced pressure, the residue was subjected to silica gel chromatography (ethyl acetate) to provide 422 mg of the title compound.

後処理

  1. customThe reaction liquid
  2. washwashed with water and saturated brine by the order
  3. dry with materialdried over magnesium sulfate
  4. distillationDistilling the solvent off under reduced pressure

出典と根拠

ORDレコード
ord-4d30b3d7fe014c9eb5cd5b761ae41e9d
出典データセット
uspto-grants-2014_09
特許番号
US08829000B2

反応ノート

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