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(-)-2-Aminobutyric acid → (s)-4-Ethyloxazolidine-2,5-dione

HRID 1173608
ノート
印刷プレビュー

反応式

HRID 1173608 の反応式
[NH2:1][C@@H:2]([CH2:6][CH3:7])[C:3]([OH:5])=[O:4].Cl[C:9](Cl)([O:11]C(=O)OC(Cl)(Cl)Cl)Cl>O1CCCC1>[CH2:6]([C@H:2]1[C:3](=[O:5])[O:4][C:9](=[O:11])[NH:1]1)[CH3:7]
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

4

反応物 2

HCID 80283(-)-2-Aminobutyric acidHCID 94429Triphosgene

生成物 1

HCID 54159673(s)-4-Ethyloxazolidine-2,5-dione収率 511%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
50 °C

実験手順

To a suspension of (2S)-2-aminobutanoic acid (10 g) and activated carbon (116 mg) in tetrahydrofuran (50 mL) was added dropwise a solution of triphosgene (10.07 g) in tetrahydrofuran (50 mL) at room temperature, and the mixture was stirred at 50° C. for 2 hr. The same experimental process was performed twice, in each of which insoluble materials were filtered off with celite, and the filtrates were combined and concentrated under reduced pressure. The residue was washed with hexane to give the title compound as a solid (yield: 22.39 g, 89%).

後処理

  1. filtrationin each of which insoluble materials were filtered off with celite
  2. concentrationconcentrated under reduced pressure
  3. washThe residue was washed with hexane

出典と根拠

ORDレコード
ord-06a822ca587e46c488715856a1c16c04
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07834051B2

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