m-Chloroperbenzoic acid → 8-Bromo-1-methyl-4-oxo-1,4-dihydroquinolin-3-yl acetate

HRID 525879ノート

反応式

HRID 525879 の反応式
C([C:4]1[C:13](=[O:14])[C:12]2[C:7](=[C:8]([Br:15])[CH:9]=[CH:10][CH:11]=2)[N:6]([CH3:16])[CH:5]=1)(=O)C.C1C=C(Cl)C=[C:19]([C:24]([O:26]O)=[O:25])C=1>ClCCl>[C:24]([O:26][C:4]1[C:13](=[O:14])[C:12]2[C:7](=[C:8]([Br:15])[CH:9]=[CH:10][CH:11]=2)[N:6]([CH3:16])[CH:5]=1)(=[O:25])[CH3:19]

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 867327443-acetyl-8-bromo-1-methylquinolin-4(1H)-one

生成物 1

HCID 867327468-Bromo-1-methyl-4-oxo-1,4-dihydroquinolin-3-yl acetate収率 87%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 3-acetyl-8-bromo-1-methylquinolin-4(1H)-one (3.4 g, 12.14 mmol) in dichloromethane (60 mL) at room temperature was added portionwise with stirring m-CPBA (4.08 g, 18.21 mmol). The resulting mixture was stirred at room temperature for 1 h. The excess m-CPBA was quenched via addition of 15% aqueous Na2SO3 (30 mL), and the resulting mixture was stirred at room temperature for 0.5 h. The layers were separated, and the organic layer was washed sequentially with water (100 mL), 5% aqueous NaHCO3 (100 mL), and brine (100 mL). The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo to afford crude 8-bromo-1-methyl-4-oxo-1,4-dihydroquinolin-3-yl acetate (3.68 g, 10.56 mmol, 87% yield) as brown solid, which was used in the next hydrolysis step without further purification. LCMS: (M+H)+: 295.9.

後処理

  1. customThe excess m-CPBA was quenched via addition of 15% aqueous Na2SO3 (30 mL)
  2. stirringthe resulting mixture was stirred at room temperature for 0.5 h
  3. customThe layers were separated
  4. washthe organic layer was washed sequentially with water (100 mL), 5% aqueous NaHCO3 (100 mL), and brine (100 mL)
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-978ea30d805445d69b34229006f0ffd0
出典データセット
uspto-grants-2016_05
特許番号
US09340556B2

反応ノート

読み込み中…