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

HRID 1967284
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HRID 1967284 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
50 °C

실험 절차

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%).

후처리

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

출처 및 근거

ORD 기록
ord-23b9573340f640fea715f44301015f24
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08420694B2

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