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Hydrochloric Acid → 3-(7-Fluoro-2-oxoquinoxalin-1(2H)-yl)propanal

HRID 1847089
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반응식

HRID 1847089 반응식
[O:1]1CCO[CH:2]1[CH2:6][CH2:7][N:8]1[C:17]2[C:12](=[CH:13][CH:14]=[C:15]([F:18])[CH:16]=2)[N:11]=[CH:10][C:9]1=[O:19].Cl.C(=O)([O-])O.[Na+]>O1CCOCC1>[F:18][C:15]1[CH:16]=[C:17]2[C:12]([N:11]=[CH:10][C:9](=[O:19])[N:8]2[CH2:7][CH2:6][CH:2]=[O:1])=[CH:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 86725012HCID 86725012, 화합물

생성물 1

HCID 867250133-(7-Fluoro-2-oxoquinoxalin-1(2H)-yl)propanal

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of 1-[2-(1,3-dioxolan-2-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one (0.6 g, 2.3 mmol) in 1,4-dioxane (6.8 ml) was added 4N hydrochloric acid (24 ml) and the mixture was stirred at room temperature for 5 hours. An aqueous solution of sodium hydrogen carbonate was added thereto and then the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure and dried under vacuum. 0.6 g (quantitative).

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후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customdried under vacuum

출처 및 근거

ORD 기록
ord-439251c57e614dbbaadf71385e554a48
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952010B2

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