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Dimethylformamide dimethyl acetal → (Z)-tert-butyl 3-((dimethylamino)methylene)-4-oxopyrrolidine-1-carboxylate

HRID 241559
ノート
印刷プレビュー

反応式

HRID 241559 の反応式
[O:1]=[C:2]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]1.[CH3:14][N:15]([CH:17](OC)OC)[CH3:16]>>[CH3:14][N:15](/[CH:17]=[C:6]1/[CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3][C:2]/1=[O:1])[CH3:16]
参加物反応条件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 78373Dimethylformamide dimethyl acetalHCID 471360Tert-butyl 3-oxopyrrolidine-1-carboxylate

生成物 1

HCID 56971730(Z)-tert-butyl 3-((dimethylamino)methylene)-4-oxopyrrolidine-1-carboxylate

反応条件

温度
105 °C

実験手順

A solution of tert-butyl 3-oxopyrrolidine-1-carboxylate (40 g, 216 mmol) was treated with DMF-DMA (267 g, 2241 mmol) and heated at 105° C. for 40 min. The solution was cooled and evaporated under reduced pressure and the resulting orange solid was treated with hexane (200 mL) and cooled in the refrigerator over the weekend. The resulting brownish-yellow solid was collected by filtration, dried and used in the next setp without further purification.

後処理

  • temperatureThe solution was cooled
  • customevaporated under reduced pressure
  • additionthe resulting orange solid was treated with hexane (200 mL)
  • temperaturecooled in the refrigerator over the weekend
  • filtrationThe resulting brownish-yellow solid was collected by filtration
  • customdried
  • customused in the next setp without further purification
  • 出典と根拠

    ORDレコード
    ord-d4c023be3a88447cba0dadf38f9eed83
    出典データセット
    uspto-grants-2014_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08653059B2

    反応ノート

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    このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート