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

HRID 1847084
ノート
印刷プレビュー

反応式

HRID 1847084 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 867250073-(6,7-Difluoro-2-oxoquinoxalin-1(2H)-yl)propanal

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-6810f85986574c9c9ee1aae7c557182b
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08952010B2

反応ノート

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