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

HRID 1967284
Notes
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Reaction equation

HRID 1967284 reaction equation
[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]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
50 °C

Procedure

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%).

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

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

Sources & evidence

ORD record
ord-23b9573340f640fea715f44301015f24
Source dataset
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08420694B2

Reaction notes

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