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Water → 1-Butyl-2-oxo-quinoline-4-carboxylic acid

HRID 6358
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인쇄 미리보기

반응식

HRID 6358 반응식
[CH2:1]([N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]([C:15]([O:17]CCCC)=[O:16])=[CH:7][C:6]1=[O:22])[CH2:2][CH2:3][CH3:4].[OH-].[Na+].O>O1CCOCC1>[CH2:1]([N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8]([C:15]([OH:17])=[O:16])=[CH:7][C:6]1=[O:22])[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 104476011-(n-Butyl)-4-(n-butyloxycarbonyl)-2-oxo-1,2-dihydro-quinoline

생성물 1

HCID 2856101-Butyl-2-oxo-quinoline-4-carboxylic acid수율 87%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A mixture of 2.04 g (6.77 mmols) of Compound b, 0.54 g of sodium hydroxide, 40 ml of water and 40 mt of dioxane was stirred at room temperature for 30 minutes. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (eluting solvent: chloroform/methanol=5/1) to give 1.44 g (yield: 87%) of Compound a.

후처리

  1. concentrationAfter concentration under reduced pressure
  2. customthe residue was purified by silica gel column chromatography (eluting solvent: chloroform/methanol=5/1)

출처 및 근거

ORD 기록
ord-0b7ac1002a9c48df9ec7bd4af81498e1
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05248684

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