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Methyl Acrylate → 3-[(2-Methoxycarbonyl-ethyl)-methyl-amino]-butyric acid methyl ester

HRID 353949
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HRID 353949 반응식
[CH3:1][O:2][C:3](=[O:9])[CH2:4][CH:5]([NH:7][CH3:8])[CH3:6].[C:10]([O:14][CH3:15])(=[O:13])[CH:11]=[CH2:12]>>[CH3:1][O:2][C:3](=[O:9])[CH2:4][CH:5]([N:7]([CH2:12][CH2:11][C:10]([O:14][CH3:15])=[O:13])[CH3:8])[CH3:6]
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참가 물질

3

반응물 2

HCID 7294Methyl AcrylateHCID 12636115Methyl 3-(methylamino)butanoate

생성물 1

HCID 220914183-[(2-Methoxycarbonyl-ethyl)-methyl-amino]-butyric acid methyl ester수율 58%

실험 절차

3-Methylamino-butyric acid methyl ester (7.6 g, 58 mmol, 1.0 equiv) was added neat to methyl acrylate (7.5 g, 87 mmol, 1.5 equiv). The resulting solution was refluxed for 16 h. The reaction was cooled and diluted with hexanes (200 mL) and an insoluble polymer separated out. The hexane solution was decanted and the polymer washed 2×100 mL hexanes with vigorous stirring. The combined hexane solutions were then concentrated in vacuo. The crude product was purified by flash chromatography on SiO2 using pure CH2Cl2 as an eluent. The pure product was isolated as a clear colorless oil (7.3 g, 58%); MS, m/z 218=M+1.

후처리

  1. temperatureThe resulting solution was refluxed for 16 h
temperature
The reaction was cooled
  • customan insoluble polymer separated out
  • customThe hexane solution was decanted
  • washthe polymer washed 2×100 mL hexanes with vigorous stirring
  • concentrationThe combined hexane solutions were then concentrated in vacuo
  • customThe crude product was purified by flash chromatography on SiO2 using pure CH2Cl2 as an eluent
  • 출처 및 근거

    ORD 기록
    ord-5d644fcf7f88461fb7cb5ea65841b42d
    출처 데이터셋
    uspto-grants-2004_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06756372B2

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