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Chloromethyl Methyl Ether → 1-Methoxymethyl-1H-imidazole-4-carboxylic acid methylester

HRID 242380
ノート
印刷プレビュー

反応式

HRID 242380 の反応式
[CH3:1][O:2][C:3]([C:5]1[N:6]=[CH:7][NH:8][CH:9]=1)=[O:4].Cl[CH2:11][O:12][CH3:13]>C(#N)C.C(OCC)(=O)C>[CH3:1][O:2][C:3]([C:5]1[N:6]=[CH:7][N:8]([CH2:11][O:12][CH3:13])[CH:9]=1)=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 7864Chloromethyl Methyl EtherHCID 178418785HCID 178418785、化合物

生成物 1

HCID 866747291-Methoxymethyl-1H-imidazole-4-carboxylic acid methylester

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

Imidazole-4-carboxylic acid methylester (5.00 g) was dissolved in acetonitrile (100 mL), and under ice cooling and stirring, were added TEA (11.1 mL) and then chloromethylmethylether (4.47 mL), followed by heating to reflux for 3 days. After being allowed to cool to room temperature, the mixture was diluted with ethyl acetate, and washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was purified by flash chromatography (methanol/chloroform=0%→7%) using silica gel column (product name: Hi-Flash Column 5 L, manufactured by Yamazen Corporation) to afford the title compound (3.64 g).

後処理

  1. temperatureby heating
  2. temperatureto reflux for 3 days
  3. washwashed with saturated brine
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe resulting residue was purified by flash chromatography (methanol/chloroform=0%→7%)

出典と根拠

ORDレコード
ord-e42ab8fdf2c6459e90fb6d0ea0ab256d
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653126B2

反応ノート

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