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Ethanol → 3,4-Dihydroxy-1-methylquinolin-2(1H)-one

HRID 1612761
ノート
印刷プレビュー

反応式

HRID 1612761 の反応式
[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[C:4](=NO)[C:3]1=[O:15].[H][H].C([OH:20])C>[Pd].Cl>[CH3:1][N:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([OH:12])=[C:4]([OH:20])[C:3]1=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 702EthanolHCID 178418361HCID 178418361、化合物HCID 178481576HCID 178481576、化合物2 回

生成物 1

HCID 546957683,4-Dihydroxy-1-methylquinolin-2(1H)-one

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 313Hydrochloric Acid溶媒

実験手順

A suspension of 1-methyl-3-oximino-quinolin-2,4(1H)-dione (1.7 gm, Formula 1.02, Example 1) and 10% palladium on charcoal (0.5 gm) in a mixture of ethanol (90 ml) and 2N hydrochloric acid (40 ml) was hydrogenated at atmospheric conditions. After 2.5 hrs no further uptake of hydrogen (510 ml) was observed. The reaction mixture was filtered and the solid cake was extracted with hot glacial acetic acid (2×100 ml). The combined filtrates were evaporated under reduced pressure and the produce was crystallized from acetic acid/water to give the title compound (1.6 gm). That the expected product was obtained was confirmed by the spectral data: MS (FAB): m/e 192 (M.+ +1); NMR (DMSO): δ3.66 (s, 3H, CH3 --N), 8.79 (s, 1H, OH), 10.16 (s, 1H, OH) ppm.

後処理

  1. filtrationThe reaction mixture was filtered
  2. extractionthe solid cake was extracted with hot glacial acetic acid (2×100 ml)
  3. customThe combined filtrates were evaporated under reduced pressure
  4. customthe produce was crystallized from acetic acid/water

出典と根拠

ORDレコード
ord-bc801b02f3114cc9a73aa81d76976dc7
出典データセット
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05190956

反応ノート

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