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Lithium Hydroxide → 3-(3,3-dimethyl-2-oxopentanoyl)-1,3-oxazolidine-4-carboxylic Acid

HRID 1250188
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HRID 1250188 반응식
[CH3:1][C:2]([CH3:18])([CH2:16][CH3:17])[C:3](=[O:15])[C:4]([N:6]1[CH:10]([C:11]([O:13]C)=[O:12])[CH2:9][O:8][CH2:7]1)=[O:5].[Li+].[OH-]>CO>[CH3:1][C:2]([CH3:18])([CH2:16][CH3:17])[C:3](=[O:15])[C:4]([N:6]1[CH:10]([C:11]([OH:13])=[O:12])[CH2:9][O:8][CH2:7]1)=[O:5]
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참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 10956210Methyl 3-(3,3-dimethyl-2-oxopentanoyl)-1,3-oxazolidine-4-carboxylate

생성물 1

HCID 101987123-(3,3-dimethyl-2-oxopentanoyl)-1,3-oxazolidine-4-carboxylic Acid수율 86.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Dissolved methyl 3-(3,3-dimethyl-2-oxopentanoyl)-1,3-oxazolidine-4-carboxylate (3) (0.6 g, 2.33 mM) in MeOH (25 ml) and added LiOH (1M in water, 10 ml, 10 mM). Stirred this mixture overnight at room temperature. Evaporated and partitioned the residues between EtOAc (50 ml) and 2N HCl (50 mL). Extracted the aqueous layer twice more with EtOAc (2×25 ml). Combined extracts, washed with brine (50 ml), dried with anhydrous magnesium sulfate, filtered and evaporated. A clear oil product (0.49 g, 86%) was obtained. Anal. (C11H17NO5) C, H, N.

후처리

  1. customEvaporated
  2. custompartitioned the residues between EtOAc (50 ml) and 2N HCl (50 mL)
  3. extractionExtracted the aqueous layer twice more with EtOAc (2×25 ml)
  4. washCombined extracts, washed with brine (50 ml)
  5. dry with materialdried with anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-41ed44af26074d948ff707cc7aa98a9e
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06337340B1

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