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Acetic Acid → HCID 178481576、化合物

HRID 1646234
ノート
印刷プレビュー

反応式

HRID 1646234 の反応式
C(O)(=O)C.[CH3:5][N:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9]([OH:16])=[CH:8][C:7]1=[O:17].[N:18]([O-])=[O:19].[Na+].CO>O.C(OCC)(=O)C>[CH3:5][N:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9](=[O:16])[C:8](=[N:18][OH:19])[C:7]1=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 176Acetic AcidHCID 887MethanolHCID 23668193Sodium NitriteHCID 546864364-Hydroxy-N-methylcarbostyril

生成物 1

HCID 178481576HCID 178481576、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8857
Ethyl Acetate
溶媒

実験手順

Glacial acetic acid (2.7 ml) was added with stirring to a solution of 1-methyl-4-hydroxy-2(1H)-quinolinone (1.75 gm) and sodium nitrite (0.8 gm) in a solvent mixture consisting of methanol (17.5 ml), ethyl acetate (20 ml) and water (10 ml) under nitrogen atmosphere. The reaction mixture was stirred for 1.5 hrs at room temperature and the organic solvents were then removed under reduced pressure. The resulting suspension was filtered and the solid washed with water to give the title compound. That the expected product was obtained was confirmed by the spectral data: MS: m/e 204 (M+); NMR (DMSO): δ3.44(s, 3H, CH3 --N), 15.34(br, 1H, =NOH) ppm.

後処理

  1. customthe organic solvents were then removed under reduced pressure
  2. filtrationThe resulting suspension was filtered
  3. washthe solid washed with water

出典と根拠

ORDレコード
ord-f711fd00135a4d699d3ca7d669fa0316
出典データセット
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05179107

反応ノート

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