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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chloromethyl Methyl Ether → 1-Methoxymethyl-1H-imidazole-4-carboxylic acid methylester

HRID 242380
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HRID 242380 반응식
[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]
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참가 물질

5

반응물 2

HCID 7864Chloromethyl Methyl EtherHCID 178418785HCID 178418785, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

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).

후처리

  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%)

출처 및 근거

ORD 기록
ord-e42ab8fdf2c6459e90fb6d0ea0ab256d
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653126B2

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