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

HRID 532529
ノート
印刷プレビュー

反応式

HRID 532529 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 obtained as such was collected by filtration, dried and used in the next step 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
  • customThe resulting brownish-yellow solid obtained
  • filtrationas such was collected by filtration
  • customdried
  • customused in the next step without further purification
  • 出典と根拠

    ORDレコード
    ord-00492b1e93bb400ea9060e37841861ea
    出典データセット
    uspto-grants-2014_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08853212B2

    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