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Hydrochloric Acid → 3-(6,7-Difluoro-2-oxoquinoxalin-1(2H)-yl)propanal

HRID 1847084
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HRID 1847084 반응식
[O:1]1CCO[CH:2]1[CH2:6][CH2:7][N:8]1[C:17]2[C:12](=[CH:13][C:14]([F:19])=[C:15]([F:18])[CH:16]=2)[N:11]=[CH:10][C:9]1=[O:20].Cl.C(=O)([O-])O.[Na+]>O1CCOCC1>[F:19][C:14]1[CH:13]=[C:12]2[C:17](=[CH:16][C:15]=1[F:18])[N:8]([CH2:7][CH2:6][CH:2]=[O:1])[C:9](=[O:20])[CH:10]=[N:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 867250061-[2-(1,3-Dioxolan-2-yl)ethyl]-6,7-difluoroquinoxalin-2(1H)one

생성물 1

HCID 867250073-(6,7-Difluoro-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]-6,7-difluoroquinoxalin-2(1H)one (0.6 g, 2.1 mmol) in dioxane (10 ml) was added 4N hydrochloric acid (10 ml) and the mixture was stirred at room temperature for 4 hours. An aqueous solution of sodium hydrogen carbonate was added thereto, the mixture was extracted with ethyl acetate, and the obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained crude product was dried in vacuum and used as such for the next step. 0.3 g (59%).

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. dry with materialthe obtained organic layer was dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe obtained crude product
  5. customwas dried in vacuum

출처 및 근거

ORD 기록
ord-6810f85986574c9c9ee1aae7c557182b
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952010B2

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