ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 427407
ノート
印刷プレビュー

反応式

HRID 427407 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

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

実験手順

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 was 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.

後処理

  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 was 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
  • 出典と根拠

    ORDレコード
    ord-da5a788188dc4caab58a25b7583794b5
    出典データセット
    uspto-grants-2001_11
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06313117B1

    反応ノート

    読み込み中…

    このページの内容参加物実験手順後処理出典と根拠反応ノート