Water → 1-Methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid

HRID 2194505노트

반응식

HRID 2194505 반응식
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([O:14]CC)=[O:13])[C:3]1=[O:17].O.[OH-].[Li+].O.C(=O)([O-])O.[Na+]>O1CCOCC1>[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([OH:14])=[O:13])[C:3]1=[O:17]

참가 물질

6

실험 절차

2.4 g (10.4 mmol) of ethyl 1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate was dissolved in 1,4-dioxane (50 mL), and 0.65 g (15 mmol) of lithium hydroxide monohydrate and 10 mL of water were added to the solution at room temperature. The resulting mixture was stirred for 24 hours at room temperature. The reaction mixture was poured into an aqueous solution of sodium hydrogen carbonate, and the mixture was washed with ethyl acetate. The aqueous phase was acidified with citric acid, and then the mixture was extracted with chloroform. The organic phase was washed with water, dried, and concentrated. The residue thus obtained was washed with ethyl acetate, and thus 2.02 g (yield: 96%) of the title compound was obtained as light yellow crystals.

후처리

  1. washthe mixture was washed with ethyl acetate
  2. extractionthe mixture was extracted with chloroform
  3. washThe organic phase was washed with water
  4. customdried
  5. concentrationconcentrated
  6. customThe residue thus obtained
  7. washwas washed with ethyl acetate

출처 및 근거

ORD 기록
ord-8f720b76a6684cdfb885a540b9da2f49
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08334236B2

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